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List of All Manufacturers & Suppliers of Polymyxin B Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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01 2Allergan Aesthetics

02 6Taro Pharmaceutical Industries

03 1Naprod Life Sciences

04 1ADRASTEA PHARMA

05 1ALTANA

06 4Actavis Inc

07 4Alcon Inc

08 2Amring Pharma

09 1Aurobindo Pharma Limited

10 20Bausch & Lomb Incorporated

11 2Bausch Health

12 2Bayer AG

13 1CAN-VET ANIMAL HEALTH SUPPLIES LTD.

14 2COMBE

15 4DELCOR ASSET

16 1Epic Pharma. LLC.

17 2Flagship Biotech International Pvt. Ltd

18 1Forest Laboratories

19 1Fresenius Kabi USA

20 1GLAND PHARMA LIMITED

21 4GSK

22 1Hanlim Pharmaceuticals Inc

23 1Harrow

24 1Health Biotech

25 1Hikma Pharmaceuticals

26 1JAMP PHARMA

27 2Jodas Expoim Pvt. Ltd

28 3Johnson & Johnson

29 2Kolmar Korea Co., Ltd.

30 1Lotus Pharmaceutical Industries

31 1Meracine

32 2NASKA

33 1NOVARTIS ANIMAL HEALTH CANADA INC

34 1Nordic Pharma

35 6Novartis Pharmaceuticals Corporation

36 2Novartis South Africa (Pty) Ltd

37 1OmniVision

38 4Padagis

39 1Perrigo Company plc

40 16Pfizer Inc

41 1Pharmacorp (Pty) Ltd

42 1Pharmaderm

43 3Pharmascience Inc.

44 1Protect Life Sciences

45 1Rising Pharmaceuticals Inc

46 1STERI-MED PHARMA INC.

47 8Sandoz B2B

48 3ScieGen Pharmaceuticals

49 1Somerset Pharmaceuticals Inc

50 1TEOFARMA Srl

51 1Vega Biotech Pvt. Ltd.

52 1VetViva Richter

53 4World Medicine

54 3XGen Pharmaceuticals

55 2Xellia Pharmaceuticals ApS

56 1Zambon Switzerland

57 1iPharma

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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

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  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Polymyxin B Sulfate

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 500000IU

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

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POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

Brand Name : POLYTRIM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

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

Packaging :

Approval Date : 1988-10-20

Application Number : 50567

Regulatory Info : DISCN

Registration Country : USA

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POLYMYXIN B SULFATE

Brand Name : POLYDERM OINTMENT USP

Dosage Form : OINTMENT

Dosage Strength : 10000UNIT/G

Packaging : 15/30/450G

Approval Date :

Application Number : 2181908

Regulatory Info : OTC

Registration Country : Canada

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POLYMYXIN B SULFATE

Brand Name : ANTIBIOTIC OINTMENT USP

Dosage Form : OINTMENT

Dosage Strength : 10000UNIT/G

Packaging : 15G

Approval Date :

Application Number : 2230251

Regulatory Info : OTC

Registration Country : Canada

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POLYMYXIN B SULFATE

Brand Name : ANTIBIOTIC CREAM FOR KIDS

Dosage Form : CREAM

Dosage Strength : 10000UNIT/G

Packaging : 15G/30G

Approval Date :

Application Number : 2315033

Regulatory Info : OTC

Registration Country : Canada

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POLYMYXIN B SULFATE

Brand Name : ORIGINAL ANTIBIOTIC CREAM

Dosage Form : CREAM

Dosage Strength : 10000UNIT/G

Packaging : 15G/30G

Approval Date :

Application Number : 2317656

Regulatory Info : OTC

Registration Country : Canada

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POLYMYXIN B SULFATE

Brand Name : ANTIBIOTIC PLUS PAIN RELIEF CREAM

Dosage Form : CREAM

Dosage Strength : 10000UNIT/G

Packaging : 15G

Approval Date :

Application Number : 2304457

Regulatory Info : OTC

Registration Country : Canada

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POLYMYXIN B SULFATE

Brand Name : COMPLETE ANTIBIOTIC OINTMENT

Dosage Form : OINTMENT

Dosage Strength : 10000UNIT/G

Packaging : 15G

Approval Date :

Application Number : 2304465

Regulatory Info : OTC

Registration Country : Canada

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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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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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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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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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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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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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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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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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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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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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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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