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01 1AbbVie Inc

02 1Allergan Aesthetics

03 1Polfa Tarchomin

04 1ADRASTEA PHARMA

05 1ALFA INTES (IND.TER.SPLENDORE)

06 1ALTANA

07 4Actavis Inc

08 5Alcon Inc

09 2Antibiotice SA

10 2BIO AGRI MIX LP

11 19Bausch & Lomb Incorporated

12 2Bausch Health

13 4Bayer AG

14 1Belfar

15 2Bharat Parenterals Limited

16 2Biodeal Pharmaceuticals

17 1Bristol Myers Squibb

18 2CAN-VET ANIMAL HEALTH SUPPLIES

19 1COMBE

20 1Chartwell Pharmaceuticals llc

21 3DELCOR ASSET

22 1DOMINION VETERINARY LABORATORIES LTD.

23 5Dong Bang Co., Ltd

24 1ENDO OPERATIONS

25 3Eli Lilly

26 1Epic Pharma. LLC.

27 2Flagship Biotech International Pvt. Ltd

28 2Fougera Pharmaceuticals Inc.

29 2GSK

30 1Glenmark Pharmaceuticals

31 1Hanlim Pharmaceuticals Inc

32 1Harrow

33 2Kolmar Korea Co., Ltd.

34 1Lannett Company, Inc.

35 1MEDIMETRIKS PHARMS

36 2Meracine

37 3Merck & Co

38 1Modern Laboratories

39 1NASKA

40 1Nostrum Laboratories

41 2Novartis Pharmaceuticals Corporation

42 1PHIBRO ANIMAL HEALTH CORPORATION

43 1PVS Laboratories

44 3Padagis

45 27Pfizer Inc

46 1Pharmacorp (Pty) Ltd

47 3Pharmaderm

48 2Qilu Animal Health Products

49 1ROXANE

50 6Sandoz B2B

51 3Saptalis pharm

52 2Savage Lab

53 2ScieGen Pharmaceuticals

54 1Seoul Pharma Co Ltd

55 1Shijiazhuang Fengqiang Animal Pharmaceutical Co., Ltd

56 2TEOFARMA Srl

57 1Teva Pharmaceutical Industries

58 1VETOQUINOL N A INC

59 2World Medicine

60 4XGen Pharmaceuticals

61 2Xepa-Soul Pattinson m SDN BHD

62 1ZRS LABS

63 1iPharma

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PharmaCompass

01

Neomycin sulphate

Brand Name : FML Neo Liquifilm Ophthalmic Suspension

Dosage Form : OPD

Dosage Strength : 5mg/ml

Packaging : 5X1mg/ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Abbvie 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

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

Regulatory Info : Dossier Available

Registration Country : Poland

Neomycin Sulfate

Brand Name :

Dosage Form : Suspension for Cutaneous Spray

Dosage Strength : 11.72MG/GM

Packaging :

Approval Date :

Application Number :

Regulatory Info : Dossier Available

Registration Country : Poland

Polfa Tarchomin

04

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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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

AACR Annual meeting
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HYDROCORTISONE; NEOMYCIN SULFATE

Brand Name : NEO-CORT-DOME

Dosage Form : CREAM;TOPICAL

Dosage Strength : 1%;EQ 3.5MG BASE/GM

Packaging :

Approval Date : 1984-06-05

Application Number : 50237

Regulatory Info : DISCN

Registration Country : USA

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06

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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HYDROCORTISONE; NEOMYCIN SULFATE

Brand Name : NEO-CORT-DOME

Dosage Form : CREAM;TOPICAL

Dosage Strength : 0.5%;EQ 3.5MG BASE/GM

Packaging :

Approval Date : 1984-06-05

Application Number : 50237

Regulatory Info : DISCN

Registration Country : USA

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07

AACR Annual meeting
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ACETIC ACID, GLACIAL; HYDROCORTISONE; NEOMYCIN SULFATE

Brand Name : NEO-CORT-DOME

Dosage Form : SUSPENSION/DROPS;OTIC

Dosage Strength : 2%;1%;EQ 0.35% BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 50238

Regulatory Info : DISCN

Registration Country : USA

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08

AACR Annual meeting
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FLURANDRENOLIDE; NEOMYCIN SULFATE

Brand Name : CORDRAN N

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 0.05%;EQ 3.5MG BASE/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50345

Regulatory Info : DISCN

Registration Country : USA

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09

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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FLURANDRENOLIDE; NEOMYCIN SULFATE

Brand Name : CORDRAN N

Dosage Form : CREAM;TOPICAL

Dosage Strength : 0.05%;EQ 3.5MG BASE/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50346

Regulatory Info : DISCN

Registration Country : USA

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10

AACR Annual meeting
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

AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

Brand Name : NEODECADRON

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 50322

Regulatory Info : DISCN

Registration Country : USA

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13

AACR Annual meeting
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AACR Annual meeting
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DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

Brand Name : NEODECADRON

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50324

Regulatory Info : DISCN

Registration Country : USA

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14

AACR Annual meeting
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AACR Annual meeting
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NEOMYCIN SULFATE; PREDNISOLONE SODIUM PHOSPHATE

Brand Name : NEO-HYDELTRASOL

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : EQ 3.5MG BASE/GM;EQ 0.25% PHOSPHATE

Packaging :

Approval Date : 1982-01-01

Application Number : 50378

Regulatory Info : DISCN

Registration Country : USA

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15

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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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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16

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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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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17

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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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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18

AACR Annual meeting
Not Confirmed
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NEOMYCIN SULFATE

Brand Name : MYCIFRADIN

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 87.5MG BASE/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 50285

Regulatory Info : DISCN

Registration Country : USA

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19

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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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

ENDO OPERATIONS

Country
AACR Annual meeting
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ENDO OPERATIONS

Country
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AACR Annual meeting
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COLISTIN SULFATE; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; THONZONIUM BROMIDE

Brand Name : COLY-MYCIN S

Dosage Form : SUSPENSION/DROPS;OTIC

Dosage Strength : EQ 3MG BASE/ML;10MG/ML;EQ 3.3MG BASE/ML;0.5MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 50356

Regulatory Info : RX

Registration Country : USA

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