Supermax

Liquid

ANTIBIOTICS
S. No.Generic NameComposition
1
CEFIXIME & LACTIC ACID BACILLUS FOR ORAL SUSPENSION
(50mg + 60 million spores)
Each 5 ml (after reconstitution) contains :

 

Cefixime Trihydrate I.P.

eq. to Anhydrous Cefixime 50 mg

Lactic Acid Bacillus 60 Million Spores

Excipients q.s.

2
CEFIXIME & POTASSIUM CLAVULANATE FOR ORAL SUSPENSION IP
(50mg+31.25mg)
Each 5 ml (after reconstitution) contains :

 

Cefixime Trihydrate I.P.

eq. to Anhydrous Cefixime 50 mg

PotassiumClavulanate IP

(as Potassium Clavulanate Diluted IP)

Eq. to Clavulanic Acid 31.25 mg

In a flavoured palatable base q.s.

Colour : Ponceau-4R

3
CEFPODOXIME PROXETIL FOR ORAL SUSPENSION IP (50mg)
Each 5 ml (after reconstitution) contains :

 

Cefpodoxime Proxetil I.P.

eq. to Cefpodoxime 50 mg

Excipients q.s.

In a flavoured palatable base Colour : Sunset Yellow FCF

4
CEFPODOXIME PROXETIL FOR ORAL SUSPENSION IP (100mg)
Each 5 ml (after reconstitution) contains :

 

Cefpodoxime Proxetil I.P.

eq. to Cefpodoxime 100 mg

Excipients q.s.

In a flavoured palatable base Colour : Sunset Yellow FCF

5
AMOXYCILLIN & POTASSIUM CLAVULANATE FOR ORAL SUSPENSION
IP (200mg+28.5mg)
Each 5 ml (after reconstitution) contains :

 

Amoxycillin Trihydrate IP

Eq. to Amoxycillin 200 mg

PotassiumClavulanate IP

(as Potassium Clavulanate Diluted IP)

Eq. to Clavulanic Acid 28.5 mg

Excipients q.s

In a flavoured palatable base

Colour : Sunset Yellow FCF

6
CEFIXIME FOR ORAL SUSPENSION 50 MG/5 ML
Each 5 ml (after reconstitution) contains :

 

Cefixime Trihydrate USP eq. to

Anhydrous Cefixime 50 mg

Excipients q.s.

Colour : Sunset Yellow FCF

7
CEFIXIME FOR ORAL SUSPENSION 25 MG/5 ML
Each 5 ml (after reconstitution) contains :

 

Cefixime Trihydrate USP eq. to

Anhydrous Cefixime 25 mg

Excipients q.s.

Colour : Sunset Yellow FCF

8
CEFIXIME & LACTIC ACID BACILLUS FOR ORAL SUSPENSION
(50mg + 20 million spores)
Each 5 ml (after reconstitution) contains :

 

Cefixime Trihydrate I.P.

eq. to Anhydrous Cefixime 50 mg

Lactic Acid Bacillus 20 Million Spores

Excipients

9
CEFIXIME & LACTIC ACID BACILLUS FOR ORAL SUSPENSION
(50mg + 60 million spores)
Each 5 ml (after reconstitution) contains :

 

Cefixime Trihydrate I.P.

eq. to Anhydrous Cefixime 50 mg

Lactic Acid Bacillus 60 Million Spores

Excipients q.s

10
CEFPODOXIME PROXETIL & POTASSIUM CLAVULANATE FOR ORAL
SUSPENSION IP (50mg+31.25mg)
Each 5 ml (after reconstitution) contains :

 

Cefpodoxime Proxetil I.P.

eq. to Cefpodoxime 50 mg

PotassiumClavulanate IP

(as Potassium Clavulanate Diluted IP)

Eq. to Clavulanic Acid 31.25 mg

Excipients q.s

In a flavoured palatable base

Colour : Sunset Yellow FCF

11
CEFPODOXIME PROXETIL & POTASSIUM CLAVULANATE FOR ORAL
SUSPENSION IP (100mg+62.5mg)
Each 5 ml (after reconstitution) contains :

 

Cefpodoxime Proxetil I.P.

eq. to Cefpodoxime 100 mg

PotassiumClavulanate IP

(as Potassium Clavulanate Diluted IP)

Eq. to Clavulanic Acid 62.5 mg

Excipients q.s

In a flavoured palatable base

Colour : Sunset Yellow FCF

12
CEFUROXIME AXEIL FOR ORAL SUSPENSION USP (125mg)
Each 5 ml (after reconstitution) contains :

 

Cefuroxime Axetil I.P.

eq. to Cefuroxime 125 mg

Excipients q.s.

Colour : Sunset Yellow FCF

13
CEFACLOR FOR ORAL SUSPENSION I.P (125mg)
Each 5 ml (after reconstitution) contains :

 

Cefaclor I.P.

eq. to anhydrous Cefaclor 125 mg

Excipients q.s.

Colour : Erythrosine

14
OFLOXACIN, METRONIDAZOLE & LACTIC ACID BACILLUS
SUSPENSION (100mg+200mg+50 million spores)
Each 5 ml contains :

 

Ofloxacin I.P. 100 mg

Metronidazole Benzoate I.P.

Eq. to Metronidazole 200 mg

Lactic Acid Bacillus 60 Million Spores

In a flavoured Syrupy Base q.s.

Colour : Sunset Yellow FCF

15
AZITHROMYCIN ORAL SUSPENSION I.P 200 MG/5 ML
Each 5 ml contains :

 

Azithromycin I.P. 200 mg

In a flavoured syrupy base q.s.

Colour : Quinoline Yellow

16
OFLOXACIN & METRONIDAZOLE ORAL SUSPENSION (100mg+200mg)
Each 5 ml contains

 

Ofloxacin i.p–100mg

Metronidazole Benzoate i.p eq. to Metronidazole–200 mg

In a flavured syrupy base q.s

Colour: tartrazine

17
NORFLOXACIN & TINIDAZOLE ORAL SUSPENSION (100mg+150mg)
Each 5 ml contains

 

Norfloxacin i.p–100mg

Tinidazole i.p–150 mg

In flavured syrupy base q.s

Colour: Sunset Yellow

18
CEFUROXIME AXETIL & POTASSIUM CLAVULANATE ORAL
SUSPENSION
Each 5 ml of reconstituted suspension contains :

 

Cefuroxime Axetil I.P.

e.q. tp Cefuroxime 125 mg

Potassium Clavulanate Diluted I.P.

e.q.to Clavulanic Acid 31.25 mg

In a Palatable suspension base q.s.

Colour : Approved colours used.

19
AZITHROMYCIN ORAL SUSPENSION 200 MG
Each 5 ml of reconstituted suspension contains :

 

Azithromycin (As Dihydrate) I.P.

e.q. to Azithromycin 200 mg

In a Palatable suspension base q.s.

Colour : Approved colours used.

20
CEFPODOXIME PROXETIL & POTASSIUM CLAVULANATE ORAL
SUSPENSION
Each 5 ml of reconstituted suspension contains :

 

Cefpodoxime Proxetil I.P.

Eq.to Cefpodoxime 50 mg

Potassium Clavulnate Diluted I.P.

Eq.to Clavulanic Acid 31.55 mg

In a Palatable suspension base q.s.

Colour : Approved colours used.

21
AMOXYCILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION I.P
(400 MG+ 57 MG)
Each 5 ml reconstituted suspension contains :

 

Amoxycillin Trihydrate I.P.

Eq. to Amoxycillin 400 mg

Potassium Clavulanate Diluted I.P.

Eq. to Clavulanic Acid 57 mg

In a Palatable suspension base q.s.

Colour : Approved colours used

22
CEPODOXINE PROXETIL & POTASSIUM CLAVULANATE ORAL
SUSPENSION
Each 5 ml of reconstituted suspension contains :

 

Cefpodoxime Proxetil I.P.

Eq.to Cefpodoxime 100 mg

Potassium Clavulnate Diluted I.P.

Eq.to Clavulanic Acid 125 mg

In a Palatable suspension base q.s.

Colour : Approved colours used.

23
AMOXYCILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION I.P
(80 MG + 11.4 MG)
Each 5 ml of reconstituted suspension contains :

 

Amoxycillin Trihydrate I.P.

e.q. to Amoxycillin 80 mg

Potassium Clavulanate Diluted I.P.

Eq. to Clavulanic Acid 11.4 mg

In a Palatable suspension base q.s.

Colour : Approved colours used.

24
AMOXYCILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION I.P
200 MG +28.5 MG)
Each 5 ml of reconstituted

 

Suspension contains

Amoxycillin Trihydrate I.P.

e.q. to Amoxycillin 200 mg

Potassium Clavulanate Diluted I.P.

Eq. to Clavulanic Acid 28.5 mg

In a Palatable suspension base q.s.

Colour : Approved colours used.

25
AZITHROMYCIN ORAL SUSPENSION I.P 100 MG/5 ML
Each 5 ml contains

 

Azithromycin i.p—100mg

In a flavured syrupy base q.s

Colour: Quinoline Yellow

26
OFLOXACIN ORAL SUSPENSION I.P 50 MG/5ML
Each 5 ml contains:

 

Ofloxacin i.p—50 mg

In a flavoured syrupy base q.s

Colour:- Sunset Yellow FCF

27
OFLOXACIN ORAL SUSPENSION I.P 100 MG/5ML
Each 5 ml contains:

 

Ofloxacin i.p—100 mg

In a flavoured syrupy base q.s

Colour:- Sunset Yellow FCF

28
AMOXYCILLIN & POTASSIUM CLAVULANATE & LACTIC ACID
BACILLUS ORAL SUSPENSION
Each 5 ml of reconsituted suspension contains:

 

Amoxycillin Trihydrate i.p eq. to A,oxycillin—200 mg

Potassium Clavulanate Diluted i.p eq. to Clavulanaic
acid—28.5 mg

Lactic acid bacillus

In a palatable suspension base–q.s

Colour: Approved colour used.

29
AMOXYCILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION
Each ml of reconsituted suspension contains:

 

Amoxycillin Trihydrate i.p eq. to Amoxycillin—80 mg

Potassium Clavulanate Diluted i.p eq. to Clavulanic acid—11.4
mg

In a palatable suspension base–q.s

Colour: Approved colour used

30
CEFPODOXIME PROXETILE ORAL SUSPENSION IP
Each ml of reconstituted suspension contains:

 

Cefpodoxime Proxetile IP

eq. to Cefpodoxime—25 mg

Excipients:q.s

Colour: Approved colour used.

31
Azithromycin Syrup
Each 5ml contains:

 

Azithromycin Dihydrate I.P

eq. to Anhydrous Azithromycin—100mg

In a flavoured sugar free base—q.s

colour: Approved colour used.

32
CEFACLOR FOR ORAL SUSPENSION I.P
Each 5 ml constitute suspension contains:

 

Cefaclor IP eq. to Anhydrous Cefaclor—125 mg

In a flavoured suspension base—q.s

Colour: Approved colour used.

33
AMOXYCILLIN FOR ORAL SUSPENSION I.P 250 mg
Each 5 ml reconstituted suspension contains :

 

Amoxycillin Trihydrate I.P.

Eq. to Amoxycillin—250 mg

Excipients—q.s

In a flavoured Palatable base

Colour: Approved colour used.

34
AMOXYCILLIN & POTASSIUM CLAVULANATE FOR ORAL SUSPENSION
I.P
Each 5 ml of reconstituted suspension contains:

 

Amoxycillin Trihydrate I.P

eq. to Amoxycillin—125 mg

Potassium Clavulanate Diluted I.P

eq. to Clavulanic Acid—31.25 mg

Excipients—q.s

In a flavoured palatable base

Colour: Approved colour used.

35
AMOXYCILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION I.P
(400 MG+ 57 MG)
Each 5 ml reconstituted suspension contains :

 

Amoxycillin Trihydrate I.P.

Eq. to Amoxycillin 400 mg

Potassium Clavulanate Diluted I.P.

Eq. to Clavulanic Acid 57 mg

In a Palatable suspension base q.s.

Colour : Approved colours used

36
AMOXYCILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION I.P
(400 MG+ 57 MG)
Each 5 ml reconstituted suspension contains :

 

Amoxycillin Trihydrate I.P.

Eq. to Amoxycillin 80 mg

Potassium Clavulanate Diluted I.P.

Eq. to Clavulanic Acid 11.4 mg

In a Palatable suspension base q.s.

Colour : Approved colours used

37
AZITHROMYCIN SUSPENSION 100 MG / 5 ML
Each 5 ml contains:

 

Azithromycin I.P—100 mg

In a flavured syrupy base—q.s

Colour: Quinoline Yellow

38
CEFIXIME FOR ORAL SUSPENSION 100 MG/5 ML IP
Each 5 ml (after reconsitution) contains:

 

Cefixime Trihydrate IP eq.

to Anhydrous Cefixime—100 mg

Excipients—q.s

Colour: Approved colour used.

39
CEFIXIME FOR ORAL SUSPENSION 25 MG/5 ML IP
Each ml (after reconsitution) contains:

 

Cefixime Trihydrate IP eq.

to Anhydrous Cefixime—25 mg

Excipients—q.s

Colour: Approved colour used.

40
AMOXYCILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION I.P
(80+11.4 MG)
Each ml of reconstituted suspension contains:

 

Amoxycillin Trihydrate I.P eq.

To Amoxycillin—80 mg

Potassium Clavulanate Diluted I.P eq.

to Clavulanic Acid—11.4 mg

in a Palatable suspension base—q.s

Colour: Approved colour used.

41
AMOXICILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION USP
Each 5 ml of reconstituted suspension contains:

 

Amoxycillin Trihydrate USP eq.

To Amoxycillin—200 mg

Potassium Clavulanate Diluted B.P eq.

to Clavulanic Acid—28.5 mg

Excipients—q.s

Colour: Approved colour used.

42
AMOXICILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION USP
Each 5 ml of reconstituted suspension contains:

 

Amoxycillin Trihydrate USP eq.

To Amoxycillin—400 mg

Potassium Clavulanate Diluted B.P eq.

to Clavulanic Acid—57 mg

Excipients—q.s

Colour: Approved colour used.

43
CEFIXIME FOR ORAL SUSPENSION USP

 

(FOR EXPORT ONLY)

Each 5 ml of reconsitituted suspension contains:

 

Cefixime Trihydrate USP eq. to Anhydrous Cefixime—100 mg

Excipients—q.s

Colour: Sunset Yellow FCF

44
CEFPODOXIME FOR ORAL SUSPENSION USP

 

(FOR EXPORT ONLY)

Each 5 ml of reconsitituted suspension contains:

 

Cefpodoxime Proxetile USP eq. to Cefpodoxime—50 mg

Excipients—q.s

In a flavoured base

Colour: Sunset Yellow FCF

45
CEFIXIME FOR ORAL SUSPENSION 50 MG/5 ML I.P
Each 5 ml (after reconsitution) contains:

 

Cefixime Trihydrate IP eq.

to Anhydrous Cefixime—50 mg

Excipients—q.s

Colour: Sunset Yellow FCF

46
AZITHROMYCIN FOR ORAL SUSPENSION USP
Each 5 ml of reconsitituted suspension contains:

 

Azithromycin USP (as dihydrate) eq. to

Azithromycin—200 mg

Excipients—q.s

47
AZITHROMYCIN USP ORAL SUSPENSION
Each 5ml of reconstituted suspension contains:

 

Azithromycin USP (as dihydrate)

eq. to Azithromycin—200 mg

Excipients–q.s

48
CIPROFLOXACIN ORAL SUSP

 

(FOR EXPORT ONLY)

Each 5 ml contains:

 

Ciprofloxacin Hydrochloride BP eq. to

Ciprofloxacin—125 mg

In a flavoured syrup base—q.s

Colour: Approved colour used

49
CIPROFLOXACIN & METRONIDAZOLE ORAL SUSP

 

(FOR EXPORT ONLY)

Each 5 ml contains:

 

Ciprofloxacin Hydrochloride BP eq. to

Ciprofloxacin—125 mg

Metronidazole Benzoate BP eq. to

Metronidazole—200 mg

In a flavoured syrup base—q.s

Colour: Approved colour used

50
AMOXYCILLIN FOR ORAL SUSP.

 

(FOR EXPORT ONLY)

Each 5 ml of reconstituted suspension contains:

 

Amoxycillin Trihydrate USP eq. to

Amoxycillin—125 mg

Excipients—q.s

Colour: Approved colour used.

51
CEFDINIR ORAL SUSPENSION IP 125 MG PER 5 ML
Each 5 ml Re-constituted suspension contains:

 

Cefdinir IP—125 mg

Excipients—q.s

Colour: Approved colour used.

52
AMOXYCILLIN 200 MG, CLAVULANIC ACID 28.5 MG AND LACTIC ACID
BACILLUS 30 MILLION SPORES DRY SYRUP
Each 5 ml unconstituted suspension contains:

 

Amoxycillin Trihydrate IP eq. to Amoxycillin—200 mg

Poptassium Clavulanate eq. to Clavulanic Acid—28.5 mg

Lactic Acid Bacillus—30 Million Spores

Excipients—q.s

Colour: Approved colour used.

53
CLARITHROMYCIN FOR ORAL SUSPENSION USP
Each 5 ml of the reconsituted suspension contains:

 

Clarithromycin I.P—125 mg

Excipients—q.s

In a flavoured base—q.s

Colour: Approved colour used.

54
LINEZOLID FOR ORAL SUSPENSION
Each 5 ml of constituted suspension contains:

 

Linezolid I.P—100 mg

Excipients—q.s

In a flavoured base

Colour: Approved colour used.

55
AMOXYCILLIN 200 MG, CLAVULANIC ACID 28.5 MG AND LACTIC ACID
BACILLUS 60 MILLION SPORES DRY SYP
Each 5 ml re-constituted suspension contains:

 

Amoxycillin Trihydrate IP eq. to

Anhydrous Amoxycillin—200mg

Potassium Clavulanate eq. to

Clavulanic Acid—28.5 mg

Lactic Acid Bacillus—60 Million Spores

Excipients—q.s

Colour: Approved colour used.

56
ERYTHROMYCIN ESTOLATE ORAL SUSPENSION USP
Each 5 ml contains:

 

Erythromycin Esolate USP eq. to Erythromycin—125 mg

Excipients—q.s

In a flavoured syrupy base—q.s

Colour: Approved colour used.

57
ERYTHROMYCIN ESTOLATE ORAL SUSPENSION USP
Each 5 ml contains:

 

Erythromycin Esolate USP eq. to Erythromycin—125 mg

Excipients—q.s

In a flavoured syrupy base—q.s

Colour: Approved colour used.

58
TRIMETHOPRIM & SULPHAMETHOXAZOLE ORAL SUSPENSION IP
Each 5 ml contains:

 

Trimethoprim IP—40 mg

Sulphamethozazole IP—200 mg

In flavoured sorbitol base—q.s

Colour: Approved colour used.

59
CEPHALEXIN FOR ORAL SUSPENSION IP
Each 5 ml of reconsituted suspension contains:

 

Cephalexin IP eq. to

Anhydrous Cephalexin—250 mg

In a flavoured base

Colour: Susnset Yellow FCF

60ERYTHROMYCIN STEARATE SUSPENSION

 

(FOR EXPORT ONLY)

Each 5 ml of the reconsituted suspension contains:

 

Erythromycin Stearate BP—200 mg

Excipients—q.s

In a flavoured base—q.s

Colour: Approved colour used.

61SULTAMICILLIN FOR ORAL SUSPENSION

 

(FOR EXPORT ONLY )

Each 5 ml of reconstituted suspension contains:

 

Sultamicilin BP—250 mg

Excipients—q.s

Colour: Approved colour used

62AMOXICILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION USP

 

( FOR EXPORT ONLY)

Each 5 ml of reconsitituted suspension contains:

 

Amoxicillin Trihydrate USP eq. to

Amoxicillin—250 mg

Potassium Clavulanate Diluted USP eq. to

Clavulanic Acid—62.5 mg

Excipients—q.s

Colour: Approved colour used.

63AMOXICILLIN & POTASSIUM CLAVULANATE ORAL SUSPENSION USP

 

( FOR EXPORT ONLY)

Each 5 ml of reconsitituted suspension contains:

 

Amoxicillin Trihydrate USP eq. to

Amoxicillin—600 mg

Potassium Clavulanate Diluted USP eq. to

Clavulanic Acid—42.9 mg

Excipients—q.s

Colour: Approved colour used.

64CEFUROXIME AXETILE FOR ORAL SUSPENSION USP

 

( FOR EXPORT ONLY)

Each 5 ml of reconstituted suspension contains:

 

Cefuroxime Axetile USP eq. to

Cefuroxime—250 mg

Excipients—q.s

Colour: Approved colour used.

65CEFADROXILFOR ORAL SUSPENSION USP 250 MG / 5 ML

 

(FOR EXPORT ONLY)

Each 5 ml of reconstituted suspension contains:

 

Cefadroxil USP eq to Cefadroxil—250 mg

Excipients—q.s

Colour: Approved colour used.

ANTIMICROBIAL AND ANTIBACTERIAL
S. No.Generic NameComposition
1
ALBENDAZOLE ORAL SUSPENSION I.P 200 MG/5 ML
Each 5 ml contains

 

Albendazole i.p—200mg

In a flavured non-syrupy base q.s

Colour: Sunset Yellow FCF

2
IVERMECTIN & ALBENDAZOLE ORAL SUSPENSION
each 10ml contains

 

Ivermectin i.p—3 mg

Albendazole i.p—400mg

In a flavured non-syrupy base q.s

Colour: Sunset yellow FCF

3
CHLORHEXADINE GLUCONATE & ISOPROPYL ALCOHOL SOLUTION
Composition:

 

Chlorhexidine Gluconate Solution IP— 2.5% w/v

(Eq. to Chlorhexidine Gluconate 0.5 %)

Isopropyl Alcohol IP— 70% v/v

In a flavoured syrypy base—q.s

Colour: Approved colour used

4
CHLORHEXIDINE MOUTH WASH I.P
Chlorhexidine Gluconate Solution I.P

 

eq. to Chlorhexadine Gluconate 0.2% w/v

Aqueous Base—q.s

Colour: Approved colour used.

5
FURAZOLIDONE ORAL SUSPENSION IP
Each 5 ml contains:

 

Furazolidone I.P—25 mg

In flavoured syrupy base

Colour: Approved colour used.

6
BENZYDAMINE HCL & CHLORHEXIDINE MOUTH WASH
Each 15 ml contains:

 

Benzydamine Hcl B.P—22.5 mg

Chlorhexidine Gluconate solution IP

eq. to Chlorhexidine—18 mg

In flavoured aqueous base

Colour: Approved colour used.

7
FURAZOLIDONE ORAL SUSPENSION USP
Each 15 ml Contains:

 

Furazolidone USP—50 mg

Excipients—q.s

In a flavoured portable base

8
BENZYDAMINE HCL & CHLORHEXIDINE MOUTH WASH
Each 5 ml contains:

 

Melatonin B.P—3 mg

In a flavoured syrupy base—q.s

colour: Approved colour used

9
CHLORHEXIDINE GLUCONATE, SODIUM FLUORIDE & ZINC
CHLORIDE MOUTHWASH
Chlorhexidine Gluconate Solution I.P

 

eq. to Chlorhexadine Gluconate 0.20% w/v

Sodium Fluoride I.P—0.05% w/v

Zinc Chloride I.P—0.09% w/v

In a plesantaly flavoured Aqueous Base—q.s

Colour: Approved colour used.

10METRONIDAZOLE ORAL SUSPEach 5ml contains:

 

Metronidazole Benzoate BP eq . To Metronidazole—200 mg

In a flavoured syrupy base—q,s

Colour: Approved colour used.

ANTIHISTAMINIC
S. No.Generic NameComposition
1
CYPROHEPTADINE HYDROCHLORIDE SYRUP I.P 2MG/5ML
Each 5ml contains

 

Cyproheptadine Hydrochloride i.p—2 mg

In a flavured sorbitol base q.s

Colour: Sunset Yellow FCF

2
CYPROHEPTADINE HYDROCHLORIDE & TRICHOLINE CITRATE SYRUP
Each 5ml contains

 

Cyproheptadine Hydrochloride i.p—2 mg

Tricholine Citrate—275mg

In a flavured sorbitol base q.s

Colour: Caramel i.p

3
FEXOFENADINE HYDROCHLORIDE ORAL SUSPENSION
Each 5 ml contains:-

 

Fexofenadine Hydrochloride i.p—30 mg

in a flavoured syrupy base q.s

Colour: Titanium Dioxide i.p

4
MONTELUKAST SODIUM & LEVOCETIRIZINE DIHYDROCHLORIDE
SYRUP
Each 5 ml contains:

 

Levocetirizine Dihydrochloride i.p –2.5 mg

Montelukast—4 mg

In a flavoured syrupy base q.s

Colour: Tartrazine

5
LEVOCETIRIZINE DIHYDROCHLORIDE SYRUP
Each 5 ml contains:

 

Levocetirizine Dihydrochloride i.p 2.5 mg

Pleasantly flavoured syrupy base q.s

Colour: Tartrazine

6
CETIRIZINE ORAL SOLUTION I.P
Each 5 ml contains:

 

Cetirizine Hydrochloride i.p 5 mg in a pleasantly flavoured
syrupy base q.s

Colour: Quinolline Yellow

7
CYPROHEPTADINE HYDROCHLORIDE & TRICHOLINE CITRATE SYRUP
Each 5ml contains:

 

Cyproheptadine Hydrochloride I.P

eq. to Anhydrous Cyproheptadine Hydrochloride—2 mg

Tricholine Citrate 65%—275 mg

In a flavoured non syrupy base—q.s

Colour: Approved colour used.

8
HYDROXYZINE ORAL SOLUTION I.P
Each 5 ml Contains:

 

Hydroxyzine Hydrochloride I.P—10 mg

In flavoured syrupy base

9
FEXOFENADINE HYDROCHLORIDE ORAL SUSPENSION
Each 5 ml contains:

 

Fexofenadine Hydrochloride I.P—30 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

10
LEVOCETIRIZINE DIHYDROCHLORIDE SYRUP
Each 5 ml contains:

 

Levocetirizine Dihydrochloride IP—5 mg

In a flavoured syrupy base

Colour: Approved colour used

11
FEXOFENADINE HYDROCHLORIDE & MONTELUKAST SODIUM
SUSPENSION
Each 5 ml contains:

 

Fexofenadine Hydrochloride I.P—30 mg

Montelukast Sodium I.P eq. to

Montelukast—4 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

12
FEXOFENADINE HYDROCHLORIDE & MONTELUKAST SODIUM
SUSPENSION
Each 5 ml contains:

 

Fexofenadine Hydrochloride I.P—60 mg

Montelukast Sodium I.P eq. to

Montelukast—4 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

13MONTELUKAST SODIUM & LEVOCETIRIZINE DIHYDROCHLORIDE SYRUPEach 5 ml contains:

 

Montelukast—4 mg

Levocetirizine Dihydrochloride IP—2.5 mg

In a falvoured surupy base—q.s

Colour: Tartrazine

ANTIPYRETIC
S. No.Generic NameComposition
1
PAEDIATRIC PARACETAMOL ORAL SUSPENSION I.P 125 MG/5 ML
Each 5ml contains

 

paracetamol i.p–125mg

In a flavured syrupy base q.s

Colour: Erythrosine

2
PAEDIATRIC PARACETAMOL ORAL SUSPENSION I.P 250 MG/5 ML
Each 5ml contains

 

paracetamol i.p–250mg

In a flavured syrupy base q.s

Colour: Erythrosine

3
PARACETAMOL PEDIATRIC ORAL SUSPENSION IP
Each ml (approx..20 drops)contains:

 

Paracetamol I.P—150 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

4
PARACETAMOL PEDIATRIC ORAL SUSPENSION IP
Each ml (approx..20 drops)contains:

 

Paracetamol I.P—150 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

5
PARACETAMOL SYRUP 125 MG/ 5 ML
Each 5 ml contains:

 

Paracetamol IP—125 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used

6
PARACETAMOL SYRUP 125 MG/ 5 ML
Each 5 ml contains:

 

Paracetamol IP—125 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used

COUGH
S. No.Generic NameComposition
1
DEXTROMETHORPHAN HYDROBROMIDE , PHENYLEPHRINE HYDROCHLORIDE
& CHLORPHENRAMINE MALEATE SYRUP
Each 5ml contains

 

Dextromethorphan hydrobromide i.p–15 mg

Phenylpherine Hydrochloride i.p–5 mg

Chlorpheniramine Maleate i.p–2 mg

In a flavured syrupy base q.s

Colour:- Ponceau-4R

2
AMBROXOL HYDROCHLORIDE, GUAIFENESIN, TERBUTALINE SULFATE
& MENTHOL SYRUP
Each 5ml contains

 

Ambroxol Hydrochloride i.p–15mg

Guaifenesin i.p—50mg

Terbutaline Sulfate i.p—1.25mg

Menthol i.p—2.5mg

In a flavuredd syrupy base q.s

Colour:- Poncea-4R

3
LEVOSULBUTAMOL SULPHATE, AMBROXOL HYDROCHLORIDE &
GUAIPHENESIN SYRUP
Each 5 ml contains:

 

Levosalbutamol Sulphate IP eq. to Levosulbutamol—0.25 mg

Ambroxol Hydrochloride I.P—7.50 mg

Guaiphenesin I.P—12.50 mg

Flavoured Syrupy Base—q,s

Colour: Approved Colour Used.

4
AMBROXOL HYDROCHLORIDE, GUAIPHENESIN & LEVOSULBUTAMOL
SYRUP
Each 5 ml contains:

 

Ambroxol Hydrochloride I.P—15 mg

Guaiphenesin I.P—50 mg

Levosulbutamol Sulphate I.P eq. to Levosulbutamol —0.5 mg

In a flavboured syrupy base—q.s

Colour: Approved Colours Used

5
BROMHEXINE HCL, DEXTROMETHORPHAN HYDROBROMIDE,
CHLORPHENIRAMINE MALEATE, GUAIFENESIN SYRUP

 

(FOR EXPORT ONLY)

Composition:

 

Chlorhexidine Gluconate Solution IP— 2.5% w/v

(Eq. to Chlorhexidine Gluconate 0.5 %)

Isopropyl Alcohol IP— 70% v/v

In a flavoured syrypy base—q.s

Colour: Approved colour used

6
AMBROXOL HYDROCHLORIDE, GUAIPHENESIN & LEVOSULBUTAMOL
SYRUP
Each 5 ml contains:

 

Ambroxol Hydrochloride I.P—30 mg

Guaiphenesin I.P—50 mg

Levosulbutamol Sulphate I.P eq. to Levosulbutamol —1 mg

In a flavoured syrupy base—q.s

Colour: Approved Colours Used

7
DEXTROMETHORPHAN HYDROBROMIDE , CHLORPHENRAMINE MALEATE
SYRUP
Each 5ml contains:

 

Dextromethrophan Hydrochloride I.P—10 mg

Chlorpheniramine Maeleate I.P—2 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

8
AMBROXOL HYDROCHLORIDE, TERBUTALINE SULPHATE, GUAIPHENESIN
SYRUP
Each 5ml contains:

 

Ambroxol Hydrochloride I.P—30 mg

Terbutaline Sulphate I.P—2.5 mg

Guaiphenesin I.P—100 mg

In a flavoured syrupy base.

Colour: Approved colour used.

9
BROMHEXINE HCL SYRUP
Each 5 ml contains:

 

Bromhexine Hcl I.P—4 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

10
NOSCAPINE, AMMONIUM CHLORIDE & SODIUM CITRATE ORAL
SUSPENSION
Each 5 ml contains:

 

Noscapine I.P—7 mg

Ammonium Chloride I.P—28 mg

Sodium Citrate I.P—3.25 mg

Flavoured syrupy base—q.s

Colour: Approved colour used.

11
ACEBROPHYLLINE, GUAIPHENESIN & TERBUTALLINE SULPHATE
SYRUP
Each 5 ml contains:

 

Acebrophylline—50 mg

Guaiphenesin IP—50 mg

Terbutaline Sulphate IP—1.25 mg

Mentholated sugar free base

Colour: Approved colour used.

12
BROMHEXINE ORAL SYRUP

 

(FOR EXPORT ONLY)

Each 5 ml contains:

 

Bromhexine Hcl BP—4 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

13
TERBUTALINE SUPHATE, BROMHEXINE HCL GUAIPHENESIN SYRUP
Each 5 ml contains:

 

Terbutaline Sulphate I.P—1.25 mg

Bromhexine Hydrochloride I.P—4 mg

Guaiphenesin I.P—50 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

14
AMBROXOL HYDROCHLORIDE, TERBUTALINE SULPHATE, GUAIPHENESIN
& MENTHOL SYRUP
Each 5 ml contains:

 

Ambroxol Hydrochloride IP—15 mg

Terbutaline Sulphate IP—1.25 mg

Guaiphenesin IP—50 mg

Menthol IP—2.5 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used

15
LEVOCLOPERASTINE FENDIZOATE ORAL SUSPENSION
Each 5 ml suspension contains:

 

Levocloperastine Fendizoate—35.4 mg

(eq. to Levocloperastine Hydrochloride)—20 mg

In a flavoured sugar free base

Excipients—q.s

Colour: Approved colour used.

ANTICOLD
S. No. Generic Name Composition
1 PARACETAMOL, PHENYLPHERINE HYDROCHLORIDE & CHLORPHENIRAMINE MALEATE SYP Each 5ml contains

Paracetamol i.p—125mg

Phenyephrine Hydrochloride i.p—2.5mg

Chlorpheniramine maleate i.p-1mg

In a flavured syrupy base q.s

Colour: sunset Yellow FCF

2 PARACETAMOL, PHENYLEPHERINE HYDCROCHLORIDE, CHLORPHENIRAMINE MALEATE, SODIUM CITRATE SYRUP Each 5 ml contains:

Paracetamol I.P—125 mg

Phenylepherine Hydrochloride I.P—5 mg

Chlorpheniramine Maeleate I.P—1 mg

Sodium Citrate I.P—60 mg

In a flavoured surupy base—q.s

Colour: Approved colours used.

3 LEVOCETIRIZINE DIHYDROCHLORIDE, AMBROXOL HYDROCHLORIDE, PARACETAMOL, PHENYLPHERINE HYDROCHLORIDE, MENTHOL SYRUP Each 5ml contains:

Levocetirizine Dihydrochloride I.P—2.5 mg

Ambroxol Hydrochloride I.P—30 mg

Paracetamol I.P—250 mg

Phenylephirine Hydrochloride I.P—5 mg

Menthol I.P—1 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

4 LEVOCETIRIZINE DIHYDROCHLORIDE, PARACETAMOL, PHENYLPHERINE HYDROCHLORIDE,SYRUP Each 5ml contains:

Levocetirizine Dihydrochloride I.P—2.5 mg

Paracetamol I.P—250 mg

Phenylephirine Hydrochloride I.P—2.5 mg

In a flavoured syrupy base—q.s

Colour: Approved colour used.

5 PARACETAMOL, PHENYLEPHRINE HCL, CHLORPHENIRAMINE MALEATE, SODIUM CITRATE & MENTHOL SUSPENSION Each 5 ml contains:

Paracetamol IP—250 mg

Phenylephrine hydrochloride IP—5 mg

Chlorpheniramine Maleate IP—2 mg

Sodium Citrate IP—60 mg

Menthol IP—1 mg

In a flavoured syrupy base—q.s

Colour: approved colour used.

6 PARACETAMOL, PHENYLEPHRINE HCL, CHLORPHENIRAMINE MALEATE, SODIUM CITRATE & MENTHOL SUSPENSION Each 5 ml contains:

Paracetamol IP—250 mg

Phenylephrine hydrochloride IP—5 mg

Chlorpheniramine Maleate IP—2 mg

Sodium Citrate IP—60 mg

Menthol IP—1 mg

In a flavoured syrupy base—q.s

Colour: approved colour used.

VITAMIN & MINERAL SUPPLEMENTS
S. No.Generic NameComposition
1
MULTIVITAMIN, MULTIMINERAL & ANTIOXIDANTS DROPS (FOR
PAEDIATRIC USE)

Each ml contains : (approx. 20 drops)

Vitamin A (As Palmitate) I.P. 2500 I.U.

Vitamin D3 I.P. 200 I.U.

Vitamin E (Tocopheryl Acetate) I.P. 5 I.U.

Vitamin B1 I.P. 1 mg

Vitamin B2 I.P. 1 mg

Vitamin B3 I.P. 10 mg

Vitamin B6 I.P. 1 mg

Vitamin C I.P. 40 mg

D-Panthenol I.P. 3 mg

Lysine Hydrochloride U.S.P. 10 mg

Chromium Chloride Hexahydrate U.S.P.

Eq. to Elemental Chromium 20 mcg

Sodium Molybdate Dihydrate B.P.

Eq. to Elemental Molybdenum 10 mcg

Sodium Selenite Pentahydrate B.P.

Eq. to Elemental Selenium 10 mcg

Zinc Sulphate I.P. 13.3 mg

In a flavoured non-syrupy base q.s.

Appropriate overages of vitamin added to compensate for loss on
storage.

2
CHOLECALCIFEROL ORAL DROPS 400 I.U

Each 0.5 ml contains :

Cholecalciferol I.P. 400 I.U.

(As Stabilized)

In a flavoured non-syrupy base q.s.

Appropriate overages of vitamin added to compensate for loss on
storage

3
POTASSIUM MAGNESIUM CITRATE WITH VITAMIN B6 ORAL SOLUTION
(978mg+14mg)

Each 5 ml contains :

Potassium Magnesium Citrate 978 mg

Pyridoxine Hydrochloride (Vit B6) I.P. 14 mg

In a flavoured non-syrupy base q.s.

Colour : Caramel I.P.

4
POTASSIUM CITRATE, MAGNESIUM CITRATE & PYRIDOXINE
HYDROCHLORIDE ORAL SOLUTION (1100mg+375mg+20mg)

Each 5 ml contains :

Potassium Citrate I.P. 1100 mg

Magnesium Citrate U.S.P. 375 mg

Pyridoxine Hydrochloride (Vit B6) I.P. 20 mg

In a flavoured non-syrupy base q.s.

Colour : Caramel I.P.

5
MULTIVITAMIN, MULTIMINERAL & ANTIOXIDANTS SYRUP (FOR
PROPHYLACTIC USE)

Each 5 ml contains :

Vitamin A (As Palmitate) I.P. 2000 I.U.

Vitamin D3 I.P. 200 I.U.

Vitamin E (Tocopheryl Acetate) I.P. 7.5 mg

Vitamin B1 I.P. 1.5 mg

Vitamin B2 I.P. 2 mg

Vitamin B6 I.P. 1 mg

Vitamin 12 I.P. 1 mcg

Vitamin C I.P. 40 mg

D-Panthenol I.P. 2.5 mg

Niacinamide I.P. 18.5 mg

Lysine Hydrochloride U.S.P. 10 mg

Lycopene U.S.P. 10% 1000 mcg

Calcium Lactate I.P.

Eq. to Elemental Calcium 1.25 mg

Potassium Iodide I.P.

eq. to Elemental Iodine 50 mcg

Chromium Chloride Hexahydrate U.S.P.

Eq. to Elemental Chromium 8 mcg

Manganese Chloride Tetrahydrate U.S.P.

Eq. to Elemental Manganese 8 mcg

Sodium Molybdate Dihydrate B.P.

Eq. to Elemental Molybdenum 8 mcg

Sodium Selenite Pentahydrate B.P.

Eq. to Elemental Selenium 10 mcg

Zinc Gluconate B.P.

Eq. to Elemental Zinc 2 mg

In a flavoured non-syrupy base q.s.

Colour : Ponceau-4R

Appropriate overages of vitamin added to compensate for loss on
storage.

6
MULTIVITAMIN & MULTIMINERAL SYRUP

Each 5 ml contains

Vitamin A (As Palmitate) i.p—1600 iu

Vitamin D3 i.p— 200 i.u

Vitamin E (Tacophenyl Acetate )i.p— 5 iu

Vitamin B1 ip— 1mg

Vitamin B2 ip—1mg

Vitamin B6 ip—1mg

Vitamin B12 p–0.5mcg

D-Panthenol i.p—1.5mg

Niacinamide i.p—15mg

Lysine Hydrochloride usp–5mg

Potassium Iodide i.p eq. to Elemental Iodine—50mcg

Chromium Chloride Hexahydrate ussp eq. to Elemental
Chromium–50mcg

Sodium Molybdate Dihydrate b.p eq. to Elemental
Molybdenum–10mcg

Sodium Selenite Pentahydrate b.p eq. to Elemental
Selenium–35mcg

Zinc Sulphate Heptahydrate i.p eq. to Elemental Zinc—11.3mg

In a flavured non-syrupy base q.s

Colour: Poncea-4R

Appropriateoverages of vitamin added to compensate for loss on
storage.

7
VITAMIN D3 (CHOLECALCIFEROL) DROPS

Each ml contains:

Cholecalciferol i.p (As Stabilized) 800 IU

In a flavured non-syrupy base q.s

Appropriate overages of vitamin added to compensate for loss on
storage.

8
LYCOPENE, VITAMIN & MINERALS SYRUP

Each 15 ml contains

Lycopene usp 10% 2000 mcg Niacinamide i.p–25 mg

Pyridoxine Hydrochloride i.p—1.5 mg

Vitamin B12 i.p— 1mcg

Folic Acid i.p— 100mcg

Biotin usp—100mcg

Copper Sulphate Pentahydrate b.p eq. to Elemental
copper—500mcg

Potassium Iodide b.p eq. to Elemental Iodide–100 mg

Magnesium Gluconate b.p eq.to Elemental Magnsium—3 mg

Sodium Selenite Pentahydrate b.p eq. to Elemental
Selenium—35mcg

Zinc Gluconate b.p eq. to Elemental Zinc–3mg

In a flavoured syrupy base q.s

Colour: Caramel USP NF

Appropriate overages of vitamin added to compensate for loss on
storage.

9
VITAMIN B-COMPLEX, CHOLINE, MINERALS WITH LYSINE SYRUP

Each 5ml contains:

Thiamine Hydrochloride i.p—2.25 mg

Riboflavine Sod. Phosphate i.p—2.5mg

Pyridoxamine Hydrochloride i.p— 1mg

Nicotinamide I, p— 22.5 mg

Cyanocobalamin I.p—2.5mcg

D-Panthenol i.p— 3mg

L-Lysine Hydrochloride usp—375mg

Choline Dihydrogen Citrate—87.5mg

Copper Sulphate Pentahydrate b.p—100 mcg

Potassium Iodide i.p—50 mg

Zinc Sulphate i.p—22.5mg

In a flavured syrupy base q.s

10
CHOLECALCIFEROL ORAL DROPS 60000 I.U

Each 5 ml contains:

Vitamin D3 (Cholecalciferol) ip 60000 iu

(In nano droplet form)

In a flavoured sugar free base q.s

Colour: Tartrazine Supara

Appropriate overages of vitamin added to compensate for loss on
storage

11
POTASSIUM MAGNESIUM CITRATE ORAL SOLUTION

Each 5ml contains:

Potassium Citrate IP 1100 mg+ Magnesium Citrate USP 375 mg
(Each ml contains approx 1 mg eq. Magmesium iron, 2 ml eq
potassium and 3 mg eq.to Citrate ion)

Colour: Caramel IP

12
MULTIVITAMIN, MULTIMINERAL & AMINOXIDANT SYRUP

Each 10 ml contains:

Methylcobalamin I.P— 1mcg

Lycopene u.s.p—10 %—100 mcg

Lysine Hydrochloride u.s.p—30 mg

Niacinamide i.p—15 mg

Zinc Sulphate i.p—3 mg

D-Panthenol i.p—2.5 mg

Vitamin A ( As Palmitate) i.p—2500 i.u

Vitamin E (Tocopheryl Acetate) i.p—5 i.u

Vitamin B2 i.p—1 mg

Vitamin B6 i.p—1 mg

Sodium Selenite Pentahydrate b.p eq. to Elemental Selenium—10
mcg

In a flavoured syrupy base–q.s

Colour: Approved colours used

Appropriate overages of vitamins added to compensate for loss
on storage

13
PROTEIN HYDROLYSATE, MULTIVITAMINS & MUTIMINERALS SYRUP

Each 5 ml contains:

Protein Hydrolysate (20% solution)— 333 mg

Iron (ferric ammonium citraye i.p)— 15 mg

Niacinamide I.P— 15 mg

L-lysin Hydrochloride USP— 3.3 mg

Magnesium Chloride I.P— 3.3 mg

D-Panthenol I.P— 2.0 mg

Vitamin B2 I.P— 1.6 mg

Vitamin B1 I.P— 1.4 mg

Vitamin B6 I.P— 0.5 mg

Zinc — 0.2 mg

(As a zinc sulphate IP)

Maganese chloride USP— 0.1 nmg

Vitamin B12 I.P— 1.0 mcg

In a flavoured syrupy base — q.s

Colour: Approved Colour Used

14
Calcium Carbonate & Vitamin D3 Suspension

Each 5ml contains:

0.625 gm of Calcium Carbonate I.P

from an organic source (oyester shell)

eq. to elemental calcium—250 mg

Vitamin D3 I.P—125 IU

In a flavoured sugar free base—q.s

Colour: Approved colour used.

15
POTASSIUM MAGNESIUM CITRATE & PYRIDOXINE HYDROCHLORDE
(VITAMIN B6 SYRUP)

Each 5ml contains:

Potassium Magnesium Citrate—978 mg

Pyridoxine Hydrochloride (Vit. B6) I.P—14mg

In a flavoured non syrupy base—q.s

Colour: Approved colour used.

16
BETA CAROTENE, ALPHA TOCOPHEROL ACETATE, CHOLECALCIFEROL,
PYRIDOXIONE HYDROCHLORIDE,
NIACINAMIDE, CYANOCOBALAMIN, BIOTIN, INOSITOL, LYSINE
HYDROCHLORIDE, MAGANESE CHLORIDE TETRAHYDRATE, SODIUM
MOLYBDATE, SODIUM SELENITE & POTASSIUM IODINE, CHROMIUM
CHLORIDE,

Each 5ml contains:

Betacarotene USP—38 mg

(As Dispersion 2.5%)

Alpha-Tocoherol Acetate I.P—5 mg

Cholecalciferol I.P—1000 IU

(As stabilized)

Pyridoxine Hydrochloride I.P—1 mg

Niacinamide I.P—15 mg

Cynocobalamin I.P—1 mcg

Biotin USP—10 mcg

Inositol USP—10 mg

L-Lysine Hydrochloride USP—30 mg

Maganese Chloride Tertahydrate USP

eq. to elemental Maganese—0.8 mg

Sodium Molybdate Dihydrate BP

eq. to elemental Molybdenum—8 mcg

Sodium Selenite Pentahydrate B.P

eq. to

17
FERROUS BIS GLYCINATE, AMINO ACID, POTASSIUM IODINE,
METHYLCOBALAMIN SUSPENSION

Each 5ml contains:

L-Methylfolate calcium 1mg

Potassium Iodine—100 mcg

Methylcobalamin—1500 mcg

Ferrous Bis Glycinate eq. to

Elemental Iron—25 mg

In a flavoured syrupy base—q.s

colour: Approved colour used.

Appropriate overages of vitamins added to compensate for loss
on storage.

18
MULTIVITAMIN, MULTIMINERALS & ANTIOXIDANT SYRUP

Each 10 ml contains:

Methlcobalamin I.P—1 mcg

Lycopene USP 10%—1000 mcg

Lysine Hydrochloride USP—30 mg

Niacinamide IP—15 mg

Zinc Sulphate I.P—3 mg

D-Panthenol I.P–2.5mg

Vitamin A (as palmitate) I.P—2500 IU

Vitamin E (Tocopheryl Acetate) IP—5 IU

Vitamin B2 IP—1 mg

Vitamin B6 IP—1 mg

Sodium Selenite Pentahydrate B.P eq. to

Elemental Selenium—10 mcg

In a flavoured syrupy base—q.s

Colour: Approved colours used.

Appropriate overages of vitamin added to compensate for loss on
storage.

19
CALCIUM CARBONATE & VITAMIN D3 SUSPENSION

Each 5 ml contains:

0.625 gm of Calcium Carbonate I.P

from an organic source (oyester shell)

eq. to elemental calcium—250 mg

Vitamin D3 I.P—125 IU

In a flavoured sugar free base–q.s

Colour: Approved colour used.

20
MULTIVITAMIN & MULTIMINERAL SYRUP

(FOR EXPORT ONLY)

Each 5ml contains:

Iron (as ferric ammonium citrate i.p)—15 mg

Niacinamide USP—15 mg

L-lysine Hydchloride USP—3.3 mg

Magnesium chloride USP—3.3 mg

D-Panthenol USP—2.0 mg

Vitamin B2 USP—1.6 mg

Vitamine B1 USP—1.4 mg

Vitamin B6 USP—0.5 mg

ZInc—0.2 mg

(as a zinc sulphate IP)

Manganese Chloride—0.1 mg

Vitamin B12 USP—1.0 mcg

In a flavoure syrupy base—q.s

Colour: Approved colour used.

21
MULTIVITAMIN WITH ZINC ORAL DROPS

Each ml contains:

Vitamins A Conentrated (oily form) IP

(as palmitate)—2500 I.U

Vitamin D3 (Cholecalciferol) IP—200 I.U

Thiamine HCL IP—0.5 mg

Riboflavin IP—0.5 mg

(as Riboflavin Sodium Phosphate)

Pyridoxine Hydrochloride IP—0.5 mg

D-Panthenol IP—1.5 mg

Nicotinamide IP—5.0 mg

Ascorbic Acid IP—25 mg

Vitamin E Acetate IP—2.5 I.U

Zinc Sulphate Monohydrate USP eq. to

elemental zinc—2.5 mg

In a flavoured base

Colour: Approved colour used.

(Appropriate overages of vitamins added to compensate for loss
of storage)

22
MULTIVITAMINS & MULTIMINERALS SYRUP

Each 15 ml (One Tablespoonful) contains:

Mecobalamin I.P—500 mcg

Vitamin B6 I.P—1.5 mg

Niacinamide I.P—45 mg

biotin USP—300 mcg

Zinc Sulphate I.P eq. to Elemental zinc—7.5 mg

Potassium Iodine I.P eq. to

Elemental Iodine—75 mcg

Ferric Ammonium Citrate I.P eq. to Elemental Iron—18 MG

Copper Sulphate Pentahydate B.P eq. to

Elemental Copper—0.45 mg

Magnaese Sulphate Monohydrate U.S.P eq. to Elemetal
Maganese—0.1 mg

Chromium Chloride U.S.P. eq. to

Elemental Chromium—25 mcg

L-Lysine Monohydratechloride U.S.P—50 mg

Sodium Selenate Pentahydrate B.P eq. to

Elemental Selenium—40 mcg

Flavoured syrupy base.—q.s

Colour: Approved colour used.

Appropriate overages of vitamins are added

23
MULTIVITAMINS & MULTIMINERALS SYRUP

Each 5 ml contains:

Vitamin A (as palmitate) IP—2500 IU

Vitamin E ( as acetate) IP—7.5 IU

Vitamin D3 IP—200 IU

Thiamine Hydrochloride IP—2.25 mg

Riboflavin IP—2.50 mg

Pyridoxine Hydrochloride IP—1 mg

Niacinamide IP—22.5 mg

Cyanocobalamin IP—2.5 mg

D-Panthenol IP—2.5 mg

Ascorbic Acid IP—40 mg

Zinc Sulphate eq. to Elemental Zinc—1 mg

Chromium Chloride USP eq. to Elemental Chromium—8 mcg

Sodium Molybdate USP eq. to Elemental Molybdenum—8 mcg

Maganese Sulphate IP eq. to Elemental Maganese—0.8 mg

Calcium Lactate IP eq. to Elemetal Calcium—1.25 mg

Sodium Selenate USP eq. to Elemental Selenium—10 mcg

Flavour syrupy base—q.s

Colour: Approved colour used.

Appropriate overages of vitamins added to compensate for loss
on storage.

24

HAEMOGLOBIN SYRUP

(FOR EXPORT ONLY)

Each 10 ml contains:

Ferric Ammonium citrate USP—250 mg

(eq. to elemental Iron 50 mg)

Thiamine Hydrochloride BP—3 mg

Pyridoxine Hydrochloride BP—1.5 mg

Cyanocobalamin BP—5 mcg

D-Panthenol USP—2.5 mg

Niacinamide USP—25 mg

In a flavoured syrupy base

Appropriate overages of vitamins added to compensate the loss
on storage

25
ZINC GLUCONATE ORAL SOLUTION 20 MG

Each ml contains

Zinc Gluconate–20 mg

In a flavured non-syrupy base q.s

Colour: Ponceau-4R

CNS
S. No.Generic NameComposition
1
SODIUM VALPORATE ORAL SOLUTION IP
Each 5 ml contains:

 

Sodium Valporate I.P— 200 mg

in flavoured sysrupy base

Colour: Approved colour used.

2
PIRACETAM SYRUP
Each 5 ml contains:

 

Piracetam I.P—500 mg

In flavoured syrupy base

Colour: Approved colour used.

3
MELATONIN SYRUP
Each 5 ml contains:

 

Melatonin B.P—3 mg

In a flavoured syrupy base—q.s

colour: Approved colour used

4
MELATONIN SYRUP
Each 15 ml contains:

 

Benzydamine Hcl B.P—22.5 mg

Chlorhexidine Gluconate solution IP

eq. to Chlorhexidine—18 mg

In flavoured aqueous base

Colour: Approved colour used.

5
PHENYTOIN ORAL SUSPENSION IP
Each ml contains:

 

Phenytoin IP—25 mg

In a flavoured base—q.s

Colour: Approved colour used.

6
PHENYTOIN ORAL SUSPENSION IP
Each ml contains:

 

Phenytoin IP—25 mg

In a flavoured base—q.s

Colour: Approved colour used.

7
RISPERIDONE ORAL SOLUTION USP
Each ml contains:

 

Risperidone I.P—1 mg

In a flavoured aqueous base

Colour: Approved colour used.

8
LEVETIRACETAM ORAL SOLUTION IP 100 MG/ML
Each 5 ml contains:

 

Levetiracetam IP—100 mg

In a flavoured syrupy base

Colour: Approved colour used.

9
SODIUM VALPORATE ORAL SOLUTION B.P.

 

(FOR EXPORT ONLY)

Each 1 ml contains:

 

Sodium Valporate B.P.—50 mg

Excipients—q.s

Colour: Approved colour used.

ANTACID
S. No.Generic NameComposition
1MAGALDRATE, OXETACAINE & SIMETHICONE ORAL SUSPENSION
(540mg+10mg+50mg+1000mg)

Each 5ml contains

Magaldrate i.p eq to Anhydrous Magaldrate–540 mg

Oxetacaine b.p– 10mg

Simethicone i.p–50 mg

Sorbitol Solution (70%) i.p-1000mg

(Non-Crystallising)

In a flavoured non-syrupy base q.s

Colour : Quinoline Yellow

2MAGALDRATE, OXETACAINE & SIMETHICONE ORAL SUSPENSION

Each 5ml contains

Magaldrate i.p eq to Anhydrous Magaldrate–540 mg

Oxetacaine b.p– 10mg

Simethicone i.p–50 mg

Sorbitol Solution (70%) i.p-1000mg

(Non-Crystallising)

In a flavoured non-syrupy base q.s

Colour : Quinoline Yellow

3
SUCRALFATE & OXETACAINE ORAL SUSPESION

Each 10ml contains

Sucralfate usp–1g

Oxetacaine bp—20mg

In a flavured palatable base q.s

Colour:- Sunset Yellow FCF

4
OXETACAINE, ALUMINIUM HYDROCHLORIDE & MAGNESIUM
HYDROCHLORIDE ORAL SUSPESION

Each 5ml contains

Oxetacaine b.p—10mg

Aluminium Hydroxide—291mg

(As dried aluminium hydroxide i.p 380mg)

Magnesium Hydroxide ip—98mg

In a flavured non-syrupy base q.s

5
SODIUM BICARBONATE ORAL SUSPENSION 1000 MG

Each 15 ml contains

Sodium Bicarbonate i.p—1000mg

In a flavured syrupy base

Colour: Tartrazine

6
MAGALDRATE & SIMETHICONE ORAL SUSPENSION I.P

Each 5ml contains

Magaldrate i.p eq to Anhydrous Magaldrate—400mg

Simethicone i.p—60mg

In a flavured non-syruy base

Colour:-Brilliant Blue FCF & Tartrazine

7
ALUMINIUM HYDROXIDE, MAGNESIUM HYDROXIDE & SIMETHICONE
ORAL SUSPENSION I.P

Each 5 ml contains

Alumimium hydroxide—250 mg

Magnesium hydroxide i.p–250 mg

Simethicone—50 mg

In flavoured non-syrupy base q.s

Colour: Brilliant Blue FCF & Tartrazine

8
SODIUM ALGINATE, SODIUM BICARBONATE & CALCIUM CARBONATE
ORAL SUSPENSION

Each 5 ml contains

Sodium Alginate i.p—250mg

Sodium Bicarbonate i.p—133.5mg

Calcium Carbonate i.p—80 mg

In a flavured non-syrupy base

approved colours used.

9
LIQUID PARAFFIN, MILK OF MAGNESIA & SODIUM PICOSULPHATE

Each 5 ml contains:

Liquid Paraffin I.P— 1.25 ml

Milk of Magnesia I.P—3.75 ml

Sodium Picosulfate B.P— 3.33 mg

In a Non Syrupy Base

Colour: Approved Colour Used.

10
ALUMINIUM, MAGNESIUM & SIMETHICONE ORAL SUSPENSION IP

Each 5 ml contains:

Aluminium Hydroxide—229.5 mg eq. to

Dried Aluminium Hydroxide Gel IP—300 mg

Magnesium Hydroxide I.P—250 mg

Simethicone I.P—40 mg

In flavoured non-syrupy base

11
DRIED ALUMINIUM HYDROXIDE, MAGNESIUM HYDROXIDE AND
QXETACAINE ORAL SUSPENSION

Each 5 ml contains:

Qxetacaine BP—10 mg

Aluminium Hydroxide—0.291 gm

(added as Aluminium Hydroxide paste eq. to 0.380 gm of

Dried Aluminium Hydroxide Gel IP)

Magnesium Hydroxide IP—98 mg

Colour: Approved colour used.

12
MAGALDRATE, SIMETHICONE & OXETACAINE ORAL SUSPENSION

Each 5 ml contains:

Magaldrate IP eq. to Anhydrous Magaldrate—480 mg

Simethicone IP—20 mg

Oxetacaine BP—10 mg

Flavoured sorbitol base

Colour: Quinoline yellow

13
DRIED ALUMINIUM HYDROXIDE GEL, MAGNESIUM HYDROXIDE
ACTIVATED DIMETHICONE & QXETACAINE SUSPENSION

Each 5 ml contains :

Aluminium Hydroxide paste eq. to

Dried Aluminium Hydroxide Gel IP—300 mg

Magnesium Hydroxide paste eq. to

Magnesium Hydroxide IP—150 mg

Acitvated Dimethicone IP—125 mg

Oxetacaine BP—10 mg

In a flavooured sugar free base—q.s

Colour: Sunset Yellow

14
SUCRALFATE & OXETACAINE SUSPESION

Each 10 ml contains:

Sucralfate USP—1000 mg

Oxetacaine BP—20 mg

In a flavoured base BP

In a flavoured base

Colour: Approved colour used.

15
ALUMINIUM HYDROXIDE, MAGNESIUM HYDROXIDE, ACTIVATED
DIMETHICONE (SIMETHICONE) & OXETACAINE ORAL SUSPENSION

Each 5ml of suspension contains:

Aluminium Hydroxide Paste eq. to

Dried Aluminium Hydroxide I.P—250 mg

Magnesium Hydroxide Paste eq. to

Magnesium Hydroxide I.P—250 mg

Activated Dimethicone I.P

(Simethicone)—50 mg

Oxetacaine B.P—10 mg

In a flavoured base—q.s

Colour: Approved colour used

16
POLYETHYLENE GLYCOL (MACROGOL 3350), SODIUM CHLORIDE,
SODIUM HYDROGEN CARBONATE & POTASSIUM CHLORIDE
CONCENTRATE FRO ORAL SOLUTION

Each 25 ml contains:

Polyethylene glycol 3350 USP—13.125 gm

Sodium Chloride I.P—0.3507 gm

Sodium Hydrogen Carbonate I.P—0.1785 gm

Potassium Chloride I.P—0.0466 gm

Excipients–q.s

17
SODIUM SULFATE+POTASSIUM SULPHATE & MAGNESIUM SULFATE
ORAL BOWEL PREPRATION SOLUTION

Each Bowel Preparation Kit Contains:

Two Bottle of each with 177 ml of oral solution.

Each Bottle with 177 ml of Bowel Preparation solution Contains:

Sodium Sulfate Anhydrous USP—17.5 g

Potassium Sulfate BP—3.13 g

Magnesium Sulfate Anhydrous USP—1.6 g

In a flavoured base

18
RANITIDINE HYDROCHLORIDE SYRUP IP

Each 5ml contains:

Ranitidine Hydrochloride IP

eq. to Ranidine—75 mg

Flavoured syrup base

Colour: Approved colour used.

19
MAGALDRATE, SIMETHICONE & DOMPERIDONE ORAL SUSP

Each 10 ml contains:

Magaldrate IP eq. to

Anhydrous magaldrate—540 mg

Simethicone IP—20 mg

Domperidone IP—10 mg

In a pleasantly flavoured sorbitol base

Colour: Approved colour used.

20
RANITIDINE ORAL SOLUTION IP

Each 5ml contains:

Ranitidine Hydrochloride IP

eq. to Ranidine—75 mg

In a flavoured syrup base

Colour: Approved colour used.

21
ALUMINIUM, MAGNESIUM & SIMETHICONE ORAL SUSPENSION IP

Each 5 ml contains

Dried Aluminium Hydroxide I.P—250 mg

Magnesium Hydroxide I.P—250 mg

Simethicone I.P—50 mg

Excipients—q.s

Colour: Approved colour used.

22

FAMOTIDINE SUSPENSION

(FOR EXPORT ONLY)

Each 5 ml contains:

Famotidine BP—10 mg

In a flavoured syrupy base

23
SUCRALFATE ORAL SUSPENSION

Each 10ml contains:

Sucralfate i.p—1g

In a flavured palatable base q.s

ANTIVIRAL
S. No.Generic NameComposition
1
ACICLOVIR ORAL SUSPENSION IP
Each 5 ml contains:

 

Aciclovir IP—200 mg

In a flavoured syrupy base

Colour: Approved colour used

DIGESTIVE SYSTEM
S. No.Generic NameComposition
1
DILL OIL, FENNEL OIL WITH SIMETHICONE ORAL DROPS
(0.005mg+0.0007mg+40mg)

Each ml contains

Dill Oil b.p–0.005ml

Fennel Oil b.p–0.0007ml

Simethicone i.p–40 mg

In a flavured palatable base q.s

2
DIGESTIVE ENZYME, DILL OIL, FENNEL OIL & SIMETHICONE
ORAL DROP

Each ml contains :

Diastase (1:1200) 33.33 mg

Pepsin (1:3000) 5 mg

Simethicone Emulsion USP

Eq. to simethicone 40 mg

Dill Oil BP 0.0002 ml

Fennel Oil U.S.P. 0.0003 ml

In a flavoured syrupy base q.s.

Colour : Sunset Yellow FCF

3
ALPHA AMYLASE & PEPSIN SYRUP

Each 5ml contains

Alpha-Amylase i.p–100 mg

(Bacterial 1800)

Pepin i.p—50 mg

In a flavured non-syrupy base q.s

Colour: Caramel USP NF

4
DIGESTIVE ENZYME, DILL OIL, FENNEL OIL & SIMETHICONE
ORAL DROP

Each ml contains:

Diastase (1:1200)—33.33mg

Pepsin (1:3000)—5mg

Simethicone Emulsion usp eq.to

Simethicone—40mg

Dill Oil b.p—0.005ml

Fennel Oil usp—0.0007ml

In aflavured syrupy base q.s

5
DIGESTIVE ENZYME WITH CARMINATIVE ORAL DROPS

Each ml contains (approx. 20 drops)

Fungal Diastase (1: 2000 ) I.P—20 mg

(Fungal Diastase deliverd from

Aspergillus-Oryazae. Digest not less

Than 40 gm. Of cooked starch

Cinnamon Oil B.P—200 mcg

Caraway Oil B.P—400 mcg

Cardamon Oil B.P—400 mcg

In a flavoured non-syrupy base—q.s

Colour: Caramel usp nf

6
FUNGAL DIASTASE & PEPSIN SYRUP

Each 5 ml contains:

Fungal Diastase I.P (1: 1200)—50 mg

(Digests not less than 60 gm of cooked starch)

Pepsin I.P (1:3000)—10 mg

(Digests not less than 30 gm of coagulate albumen)

Sorbitol Solution (70%)—q.s

In a flavoured palatable base

Colour: Approved colour used.

7
ALPHA-AMYLASE & PAPAIN SYRUP

Each 5 ml contains:

Alpha-Amylase IP—100 mg

(Bacterial 1: 800)

Papain IP—50 mg

In a flavoured non-syrupy baes—q.s

Colour: Approved colour used.

LAXATIVE
S. No.Generic NameComposition
1
LACTULOSE SOLUTION USP 3.350 G

Each 5 ml contains

Lactulose Concentrate usp eq.to Lactulose— 3.350g

In a palatable non-syrupy base q.s

Colour:Caramel i.p

2
POLYERHYLENE GLYCOL ORAL LAXATIVE LIQUID

Each 25 ml contains:

Polyethylene glycol 4000 i.p—10mg

Excipients–q.s

3
LACTULOSE SOLUTION USP

Each 15 ml contains:

Lactulose Concentrate U.S.P—10 g

In a palatable non-syrupy base—q.s

colour: Approved colour used.

4LACTULOSE SOLUTION

Each 15 ml contains:

Lactulose Concentrate U.S.P—10 gm

In a palatable non-syrupy base—q.s

colour: Approved colour used.

ANTIEMETIC
S. No.Generic NameComposition
1
ONDASNSETRON ORAL SOLUTION I.P
Each 5 ml contains:-

 

Ondansetron Hydrochloride i.p eq. to Ondansetron— 2 mg

In a flavured syrupy base q.s

Colour:- Ponceau-4R

2
DOMPERIDONE SUSPENSION I.P
Each 5ml contains:

 

Domperidone i.p—5 mg

In a flavoured syrupy base q.s

Colour: Sunset Yellow FCF

3
ONDANSETRON ORAL SOLUTION USP

 

(FOR EXPORT ONLY)

Eachn 5 ml contains:

 

Ondansetron Hydrochloride USP eq. to

Ondansetron—4 mg

In a flavoured syrupy base

4ONDANSETRON ORAL SOLUTION USP

 

(FOR EXPORT ONLY)

Eachn 5 ml contains:

 

Ondansetron Hydrochloride USP eq. to

Ondansetron—2 mg

In a flavoured syrupy base

ANTIFUNGAL
S. No.Generic NameComposition
1
POSACONAZOLE ORAL SUSPENSION 40
Each 5 ml contains:

 

Posaconazole—40 mg

Sodium Benzoate I.P—2 mg

In a flavoured palatable base—q.s

Colour: Approved Colour Used.

URINARY DISORDER
S. No.Generic NameComposition
1
DI-SODIUM HYDROGEN CITRATE SYRUP
Each 5ml contains

 

Disodium Hydrogen Citrate B.P—1.4 g

In a palatable non-syrupy base

Colour: Tartrazine

2
NITROFURANTOIN SUSPENSION
Each 5 ml contains:

 

Nitrofurantoin IP—25 mg

Flavoured syrupy base—q.s

Colou: Approved colour used.

IRON SUPPLEMENT
S. No.Generic NameComposition
1
FERROUS ASCORBATE & FOLIC ACID ORAL SUSPENSION 
(30mg+550mcg)

Each 5 ml contains :

Ferrous Ascorbate

eq. to Elemental Iron 30 mg

Folic Acid I.P. 550 mcg

In a flavoured syrupy base q.s.

Colour : Erythrosine

Appropriate overages of vitamin added to compensate for loss on
storage.

2
FERRIC AMMONIUM CITRATE, FOLIC ACID, CYNOCOBALAMIN SYRUP

Each 5ml contains:

Ferric Ammonium Citrate I.P—160 mg

(eq. to 33 mg of elemental iron)

Folic Acid I.P—1mg

Cynocobalamin I.P—7.5 mcg

In a flavoured syrupy base—q.s

Colour: Approved Colours Used.

3
FERRIC AMMONIUM CITRATE, FOLIC ACID, CYNOCOBALAMIN SYRUP

Each 5ml contains:

Ferric Ammonium Citrate I.P—200 mg

(eq. to 40 mg of elemental iron)

Folic Acid I.P—1mg

Cynocobalamin I.P—7.5 mcg

In a flavoured syrupy base—q.s

Colour: Approved Colours Used.

4
FERROUS FUMARATE, FOLIC ACID, CYANOCOBALAMIN SYRUP 

Each 5 ml contains:

Ferrous Fumarate IP eq. to

Elemental iron—100 mg

Folic Acid IP—0.5 mg

Cyanocobalamin (Vit. B12) IP—5 mcg

Flavoured syrupy base—q.s

Colour: Approved colour used.

Appropriate overags added to compensate for loss on storage.

CORTICOSTEROID
S. No.Generic NameComposition
1
DEFLAZACORT ORAL SUSPENSION
Each 5 ml contains:-

 

Deflazacort—6 mg

in a flavoured syrupy base q.s

Colour: Quinoline Yellow

PREBIOTICS
S. No.Generic NameComposition
1
PREBIOTIC & PROBIOTIC FOR ORAL SUSPENSION

Each 5 ml (after reconstitution) contains:

Lactobacillus Acidophilus—0.2 Billion Spores

Lactobacillus Rhamnosus—0.2 Billion Spores

Bifidobacterium Longum—0.2 Billion Spores

Bifidobacterium Bifidus—0.125 Billion Spores

Saccharomyces Boulardii—0.025 Billion Spores

Fructo-Oligosaccharides—25 mg

Excipients—q.s

Colour: Sunset Yellow FCF