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01 1Sanofi

02 2Allergan Aesthetics

03 12care4

04 1ALTANA

05 4Actavis Inc

06 1Adastra Pharmaceuticals

07 1Akorn Pharmaceuticals

08 5Alcon Inc

09 1Aurobindo Pharma Limited

10 22Bausch & Lomb Incorporated

11 2Bausch Health

12 2Bayer AG

13 1CAN-VET ANIMAL HEALTH SUPPLIES

14 2COMBE

15 4DELCOR ASSET

16 3Ebb Medical

17 1Epic Pharma. LLC.

18 1Europharma

19 2Flagship Biotech International Pvt. Ltd

20 1Forest Laboratories

21 1Fresenius Kabi USA

22 1GLAND PHARMA LIMITED

23 5GSK

24 2Grupo Farmasierra S.L

25 1Hanlim Pharmaceuticals Inc

26 1Harrow

27 1Health Biotech

28 1Hikma Pharmaceuticals

29 2Jodas Expoim Pvt. Ltd

30 3Johnson & Johnson

31 2Kolmar Korea Co., Ltd.

32 1Laboratorios Salvat

33 1Lotus Pharmaceutical Industries

34 1M4 Pharma Sl

35 2Medartuum

36 1Meracine

37 2NASKA

38 1NOVARTIS ANIMAL HEALTH CANADA INC

39 1Naprod Life Sciences

40 1NordMedica

41 7Novartis Pharmaceuticals Corporation

42 2Novartis South Africa (Pty) Ltd

43 3ORIFARM GROUP AS

44 1OmniVision

45 1Omnia L?kemedel Ab

46 4Padagis

47 1Paranova Pharmaceuticals Ab

48 1Perrigo Company plc

49 18Pfizer Inc

50 1Pharmaceutical Laboratory Sit - Hygienic Therapeutic Specialties Srl

51 1Pharmacorp (Pty) Ltd

52 1Pharmaderm

53 3Pharmascience Inc.

54 1Protect Life Sciences

55 1Reig Jofre

56 1Rising Pharmaceuticals Inc

57 1S.A. Alcon-Couvreur N.V.

58 1STERI-MED PHARMA INC.

59 8Sandoz B2B

60 1Saptalis pharm

61 5ScieGen Pharmaceuticals

62 1Somerset Pharmaceuticals Inc

63 1TEOFARMA Srl

64 6Taro Pharmaceutical Industries

65 1Teofarma

66 1Teva Pharmaceutical Industries

67 1Themis Medicare

68 1Tora Laboratories Slu

69 1Vega Biotech Pvt. Ltd.

70 1VetViva Richter

71 4World Medicine

72 3XGen Pharmaceuticals

73 2Xellia Pharmaceuticals ApS

74 1Zambon Switzerland

75 1iPharma

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Allowed

Registration Country : Switzerland

Diphtheria Toxoid; Tetanus Toxoid; Bordetella Pertussis Antigen; Inactivated Poliovirus Types 1, 2, 3; Diphtheria Toxoid; Tetanus Toxoid; Bordetella Pertussis Antigen; Inactivated Poliovirus Types 1, 2, 3; Polymyxin B; Haemophilus Influenzae Type B Polysaccharide Conjugated With Tetanus Toxoid; Pertussis Fimbriae

Brand Name : Adacel-Polio

Dosage Form : Suspension For Injection

Dosage Strength :

Packaging :

Approval Date : 26/08/2022

Application Number : 68110

Regulatory Info : Allowed

Registration Country : Switzerland

Sanofi Company Banner

02

NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PREDNISOLONE ACETATE

Brand Name : POLY-PRED

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.35% BASE;10,000 UNITS/ML;0.5%

Packaging :

Approval Date : 1982-01-01

Application Number : 50081

Regulatory Info : DISCN

Registration Country : USA

Abbvie CB

03

POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

Brand Name : POLYTRIM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1988-10-20

Application Number : 50567

Regulatory Info : DISCN

Registration Country : USA

Abbvie CB

04

PREP
Not Confirmed
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PREP
Not Confirmed

NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : STATROL

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50344

Regulatory Info : DISCN

Registration Country : USA

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05

PREP
Not Confirmed
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PREP
Not Confirmed

NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : STATROL

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 3.5MG BASE/ML;16,250 UNITS/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 50456

Regulatory Info : DISCN

Registration Country : USA

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06

PREP
Not Confirmed
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PREP
Not Confirmed

GRAMICIDIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : NEO-POLYCIN

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.025MG/ML;EQ 1.75MG BASE/ML;10,000 UNITS/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 60427

Regulatory Info : DISCN

Registration Country : USA

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07

PREP
Not Confirmed
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PREP
Not Confirmed

BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : CORTISPORIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 50416

Regulatory Info : DISCN

Registration Country : USA

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08

PREP
Not Confirmed
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PREP
Not Confirmed

BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : LUMI-SPORYN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50417

Regulatory Info : RX

Registration Country : USA

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09

PREP
Not Confirmed
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PREP
Not Confirmed

BACITRACIN ZINC; POLYMYXIN B SULFATE

Brand Name : POLYSPORIN

Dosage Form : AEROSOL;TOPICAL

Dosage Strength : 10,000 UNITS/GM;2,000,000 UNITS/GM

Packaging :

Approval Date : 1985-03-01

Application Number : 50167

Regulatory Info : DISCN

Registration Country : USA

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10

PREP
Not Confirmed
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PREP
Not Confirmed

NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : NEOSPORIN

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1985-01-14

Application Number : 50176

Regulatory Info : DISCN

Registration Country : USA

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11

PREP
Not Confirmed
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PREP
Not Confirmed

DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : MAXITROL

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 50023

Regulatory Info : RX

Registration Country : USA

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12

PREP
Not Confirmed
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PREP
Not Confirmed

BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : CORTISPORIN

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1984-05-04

Application Number : 50168

Regulatory Info : DISCN

Registration Country : USA

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13

PREP
Not Confirmed
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PREP
Not Confirmed

HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : CORTISPORIN

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 50169

Regulatory Info : DISCN

Registration Country : USA

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14

PREP
Not Confirmed
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PREP
Not Confirmed

CHLORAMPHENICOL; HYDROCORTISONE ACETATE; POLYMYXIN B SULFATE

Brand Name : OPHTHOCORT

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 10MG/GM;5MG/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50201

Regulatory Info : DISCN

Registration Country : USA

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15

PREP
Not Confirmed
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PREP
Not Confirmed

CHLORAMPHENICOL; POLYMYXIN B SULFATE

Brand Name : CHLOROMYXIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 1%;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50203

Regulatory Info : DISCN

Registration Country : USA

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16

PREP
Not Confirmed
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PREP
Not Confirmed

HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : CORTISPORIN

Dosage Form : CREAM;TOPICAL

Dosage Strength : 0.5%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1985-08-09

Application Number : 50218

Regulatory Info : DISCN

Registration Country : USA

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17

PREP
Not Confirmed
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PREP
Not Confirmed

HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : CORTISPORIN

Dosage Form : SOLUTION/DROPS;OTIC

Dosage Strength : 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 50479

Regulatory Info : DISCN

Registration Country : USA

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18

PREP
Not Confirmed
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PREP
Not Confirmed

GRAMICIDIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : NEOSPORIN

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.025MG/ML;EQ 1.75MG BASE/ML;10,000 UNITS/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 60582

Regulatory Info : RX

Registration Country : USA

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19

PREP
Not Confirmed
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PREP
Not Confirmed

DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : MAXITROL

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 0.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50065

Regulatory Info : RX

Registration Country : USA

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20

COMBE

Country
PREP
Not Confirmed
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COMBE

Country
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PREP
Not Confirmed

BACITRACIN; POLYMYXIN B SULFATE

Brand Name : LANABIOTIC

Dosage Form : DISC;TOPICAL

Dosage Strength : 500 UNITS/GM;5,000 UNITS/GM

Packaging :

Approval Date : 1986-09-22

Application Number : 50598

Regulatory Info : DISCN

Registration Country : USA

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