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01 1XELLIA PHARMS APS

02 2ALLERGAN

03 3ALCON

04 1ALCON PHARMS LTD

05 1ALTANA

06 2AMNEAL

07 9BAUSCH AND LOMB

08 4CASPER PHARMA LLC

09 2COMBE

10 2DOW PHARM

11 1EPIC PHARMA LLC

12 1EUGIA PHARMA

13 1FOREST LABS

14 1FRESENIUS KABI USA

15 1GLAND

16 3GLAXOSMITHKLINE

17 1HARROW EYE

18 1HIKMA

19 1IPHARM

20 9MONARCH PHARMS

21 2NASKA

22 2NOVARTIS

23 4PADAGIS US

24 1PADDOCK LLC

25 1PARKE DAVIS

26 1PARKEDALE

27 2PFIZER

28 1PHARMACIA AND UPJOHN

29 1PHARMADERM

30 11PHARMAFAIR

31 1PHARMOBEDIENT

32 1RISING

33 6SANDOZ

34 1SAPTALIS PHARMS

35 2SCHERING

36 5SCIEGEN PHARMS

37 1SOMERSET THERAPS LLC

38 4WATSON LABS

39 1X GEN PHARMS

40 2XGEN PHARMS

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PharmaCompass

01

POLYMYXIN B SULFATE

Brand Name : POLYMYXIN B SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500,000 UNITS BASE/VIAL

Approval Date : 2014-01-15

Application Number : 202766

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

Company Banner

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Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1988-10-20

Application Number : 50567

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie CB

04

RDD
Not Confirmed
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RDD
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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05

RDD
Not Confirmed
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RDD
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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06

RDD
Not Confirmed
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RDD
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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07

RDD
Not Confirmed
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RDD
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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08

RDD
Not Confirmed
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RDD
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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09

RDD
Not Confirmed
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RDD
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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10

RDD
Not Confirmed
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RDD
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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