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01 1Sanofi

02 2Allergan Aesthetics

03 12care4

04 1ALTANA

05 4Actavis Inc

06 1Adelco-Chromatourgia Anthinon E. Colocotronis Bros S.A.

07 1Akorn Pharmaceuticals

08 5Alcon Inc

09 2Amneal Pharmaceuticals

10 1Aurobindo Pharma Limited

11 22Bausch & Lomb Incorporated

12 2Bausch Health

13 2Bayer AG

14 1CAN-VET ANIMAL HEALTH SUPPLIES

15 2CHANELLE PHARMACEUTICALS MANUFACTURING LIMITED

16 2COMBE

17 4DELCOR ASSET

18 3Ebb Medical

19 1Epic Pharma. LLC.

20 1Europharma

21 2Flagship Biotech International Pvt. Ltd

22 1Forest Laboratories

23 1Fresenius Kabi USA

24 1GLAND PHARMA LIMITED

25 5GSK

26 2Grupo Farmasierra S.L

27 1Hanlim Pharmaceuticals Inc

28 1Harrow

29 1Health Biotech

30 1Hikma Pharmaceuticals

31 2Jodas Expoim Pvt. Ltd

32 3Johnson & Johnson

33 2Kolmar Korea Co., Ltd.

34 1Laboratorios Salvat

35 1Lotus Pharmaceutical Industries

36 1M4 Pharma Sl

37 2Medartuum

38 1Meracine

39 2NASKA

40 1NOVARTIS ANIMAL HEALTH CANADA INC

41 1Naprod Life Sciences

42 1NeoFarma Pharmaceuticals Limited

43 1NordMedica

44 10Novartis Pharmaceuticals Corporation

45 2Novartis South Africa (Pty) Ltd

46 5ORIFARM GROUP AS

47 1OmniVision

48 1Omnia L?kemedel Ab

49 1PHARMOBEDIENT

50 4Padagis

51 1Paranova Pharmaceuticals Ab

52 1Perrigo Company plc

53 22Pfizer Inc

54 1Pharmaceutical Laboratory Sit - Hygienic Therapeutic Specialties Srl

55 1Pharmacorp

56 1Pharmaderm

57 3Pharmascience Inc.

58 1Protect Life Sciences

59 1Reig Jofre

60 1Rising Pharmaceuticals Inc

61 1S.A. Alcon-Couvreur N.V.

62 8Sandoz B2B

63 1Saptalis pharm

64 5ScieGen Pharmaceuticals

65 1Somerset Pharmaceuticals Inc

66 1Steri-Med Pharma

67 1TEOFARMA Srl

68 6Taro Pharmaceutical Industries

69 1Teofarma

70 1Teva Pharmaceutical Industries

71 1Themis Medicare

72 1Tora Laboratories Slu

73 1Vega Biotech Pvt. Ltd.

74 2VetViva Richter

75 5World Medicine

76 3XGen Pharmaceuticals

77 2Xellia Pharmaceuticals ApS

78 2Zambon Switzerland

79 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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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VMX
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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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VMX
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
VMX
Not Confirmed
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COMBE

Country
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VMX
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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