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01 2ALLERGAN

02 1ACTAVIS LABS FL INC

03 1ADRASTEA PHARMA

04 3ALCON

05 1ALCON PHARMS LTD

06 1ALTANA

07 2AMRING PHARMS

08 9BAUSCH AND LOMB

09 4CASPER PHARMA LLC

10 2COMBE

11 2DOW PHARM

12 1EPIC PHARMA LLC

13 1EUGIA PHARMA

14 1FOREST LABS

15 1FRESENIUS KABI USA

16 1GLAND

17 3GLAXOSMITHKLINE

18 1HARROW EYE

19 1HIKMA

20 1IPHARM

21 9MONARCH PHARMS

22 2NASKA

23 1NORDIC PHARMA

24 2NOVARTIS

25 4PADAGIS US

26 1PADDOCK LLC

27 1PARKE DAVIS

28 1PARKEDALE

29 2PFIZER

30 1PHARMACIA AND UPJOHN

31 1PHARMADERM

32 11PHARMAFAIR

33 1RISING

34 6SANDOZ

35 2SCHERING

36 3SCIEGEN PHARMS INC

37 1SOMERSET THERAPS LLC

38 3WATSON LABS

39 1X GEN PHARMS

40 1XELLIA PHARMS APS

41 2XGEN PHARMS

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PharmaCompass

01

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Antibody Engineering
Not Confirmed

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%

Approval Date : 1982-01-01

Application Number : 50081

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Abbvie CB

02

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Antibody Engineering
Not Confirmed

POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

Brand Name : POLYTRIM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

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

Approval Date : 1988-10-20

Application Number : 50567

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie CB

03

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Antibody Engineering
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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