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01 2Allergan Aesthetics

02 1Naprod Life Sciences

03 1ADRASTEA PHARMA

04 1ALTANA

05 4Actavis Inc

06 1Akorn Pharmaceuticals

07 4Alcon Inc

08 1Aurobindo Pharma Limited

09 21Bausch & Lomb Incorporated

10 2Bausch Health

11 2Bayer AG

12 1CAN-VET ANIMAL HEALTH SUPPLIES

13 2COMBE

14 4DELCOR ASSET

15 1Epic Pharma. LLC.

16 2Flagship Biotech International Pvt. Ltd

17 1Forest Laboratories

18 1Fresenius Kabi USA

19 1GLAND PHARMA LIMITED

20 4GSK

21 1Hanlim Pharmaceuticals Inc

22 1Harrow

23 1Health Biotech

24 1Hikma Pharmaceuticals

25 1JAMP PHARMA

26 2Jodas Expoim Pvt. Ltd

27 3Johnson & Johnson

28 2Kolmar Korea Co., Ltd.

29 1Lotus Pharmaceutical Industries

30 1Meracine

31 2NASKA

32 1NOVARTIS ANIMAL HEALTH CANADA INC

33 6Novartis Pharmaceuticals Corporation

34 2Novartis South Africa (Pty) Ltd

35 1OmniVision

36 4Padagis

37 1Perrigo Company plc

38 16Pfizer Inc

39 1Pharmacorp (Pty) Ltd

40 1Pharmaderm

41 3Pharmascience Inc.

42 1Protect Life Sciences

43 1Rising Pharmaceuticals Inc

44 1STERI-MED PHARMA INC.

45 8Sandoz B2B

46 3Saptalis pharm

47 3ScieGen Pharmaceuticals

48 1Somerset Pharmaceuticals Inc

49 1TEOFARMA Srl

50 6Taro Pharmaceutical Industries

51 1Themis Medicare

52 1Vega Biotech Pvt. Ltd.

53 1VetViva Richter

54 4World Medicine

55 3XGen Pharmaceuticals

56 2Xellia Pharmaceuticals ApS

57 1Zambon Switzerland

58 1iPharma

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PharmaCompass

01

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

02

  • 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

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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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
AACR Annual meeting
Not Confirmed
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COMBE

Country
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AACR Annual meeting
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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