Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 4,449Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 2Allergan Aesthetics

02 1ALTANA

03 4Actavis Inc

04 1Adastra Pharmaceuticals

05 1Akorn Pharmaceuticals

06 4Alcon Inc

07 1Aurobindo Pharma Limited

08 22Bausch & Lomb Incorporated

09 2Bausch Health

10 2Bayer AG

11 1CAN-VET ANIMAL HEALTH SUPPLIES

12 2COMBE

13 4DELCOR ASSET

14 1Epic Pharma. LLC.

15 2Flagship Biotech International Pvt. Ltd

16 1Forest Laboratories

17 1Fresenius Kabi USA

18 1GLAND PHARMA LIMITED

19 4GSK

20 1Hanlim Pharmaceuticals Inc

21 1Harrow

22 1Health Biotech

23 1Hikma Pharmaceuticals

24 1JAMP PHARMA

25 2Jodas Expoim Pvt. Ltd

26 3Johnson & Johnson

27 2Kolmar Korea Co., Ltd.

28 1Lotus Pharmaceutical Industries

29 1Meracine

30 2NASKA

31 1NOVARTIS ANIMAL HEALTH CANADA INC

32 1Naprod Life Sciences

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

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

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

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Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

03

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

04

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

05

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

06

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

07

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

08

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
Not Confirmed

HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : CASPORYN HC

Dosage Form : SUSPENSION/DROPS;OTIC

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

Packaging :

Approval Date : 1982-01-01

Application Number : 60613

Regulatory Info : RX

Registration Country : USA

blank

09

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

10

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

11

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

12

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

13

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

14

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

15

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

16

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

17

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

18

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

19

IFT FIRST
Not Confirmed
arrow
arrow
IFT FIRST
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

blank

20

COMBE

Country
IFT FIRST
Not Confirmed
arrow

COMBE

Country
arrow
IFT FIRST
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

blank