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01 2ALLERGAN

02 1ADRASTEA PHARMA

03 3ALCON

04 1ALCON PHARMS LTD

05 1ALTANA

06 9BAUSCH AND LOMB

07 4CASPER PHARMA LLC

08 2COMBE

09 2DOW PHARM

10 1EPIC PHARMA LLC

11 1EUGIA PHARMA

12 1FOREST LABS

13 1FRESENIUS KABI USA

14 1GLAND

15 3GLAXOSMITHKLINE

16 1HARROW EYE

17 1HIKMA

18 1IPHARM

19 9MONARCH PHARMS

20 2NASKA

21 2NOVARTIS

22 4PADAGIS US

23 1PADDOCK LLC

24 1PARKE DAVIS

25 1PARKEDALE

26 2PFIZER

27 1PHARMACIA AND UPJOHN

28 1PHARMADERM

29 11PHARMAFAIR

30 1RISING

31 6SANDOZ

32 3SAPTALIS PHARMS

33 2SCHERING

34 3SCIEGEN PHARMS INC

35 1SOMERSET THERAPS LLC

36 4WATSON LABS

37 1X GEN PHARMS

38 1XELLIA PHARMS APS

39 2XGEN PHARMS

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PharmaCompass

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Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1988-10-20

Application Number : 50567

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie CB

03

Process Development
Not Confirmed
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Process Development
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

Approval Date : 1985-03-01

Application Number : 50167

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Process Development
Not Confirmed
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Process Development
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

Approval Date : 1985-01-14

Application Number : 50176

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Process Development
Not Confirmed
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Process Development
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

Approval Date : 1982-01-01

Application Number : 50023

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AT

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06

Process Development
Not Confirmed
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Process Development
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**

Approval Date : 1984-05-04

Application Number : 50168

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

Process Development
Not Confirmed
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Process Development
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

Approval Date : 1982-01-01

Application Number : 50169

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

Process Development
Not Confirmed
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Process Development
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

Approval Date : 1982-01-01

Application Number : 50201

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Process Development
Not Confirmed
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Process Development
Not Confirmed

CHLORAMPHENICOL; POLYMYXIN B SULFATE

Brand Name : CHLOROMYXIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 1%;10,000 UNITS/GM

Approval Date : 1982-01-01

Application Number : 50203

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

Process Development
Not Confirmed
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Process Development
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

Approval Date : 1982-01-01

Application Number : 50065

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AT

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