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01 1ALLERGAN

02 1ACTAVIS LABS FL INC

03 1ADRASTEA PHARMA

04 3ALCON

05 2ALCON PHARMS LTD

06 1ALTANA

07 8BAUSCH AND LOMB

08 3BAYER PHARMS

09 1BRISTOL MYERS SQUIBB

10 3CASPER PHARMA LLC

11 1CHARTWELL MOLECULAR

12 1COMBE

13 2DOW PHARM

14 1ENDO OPERATIONS

15 1EPIC PHARMA LLC

16 2FOUGERA

17 1GLAXOSMITHKLINE

18 1HARROW EYE

19 1IPHARM

20 1LANNETT

21 3LILLY

22 1MEDIMETRIKS PHARMS

23 3MERCK

24 8MONARCH PHARMS

25 1NASKA

26 1NOSTRUM LABS INC

27 2NOVARTIS

28 3PADAGIS US

29 1PFIZER

30 18PHARMACIA AND UPJOHN

31 3PHARMADERM

32 11PHARMAFAIR

33 1ROXANE

34 6SANDOZ

35 3SAPTALIS PHARMS

36 2SAVAGE LABS

37 1SCHERING

38 2SCIEGEN PHARMS INC

39 1TEVA

40 3WATSON LABS

41 2X GEN PHARMS

42 2XGEN PHARMS

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PharmaCompass

01

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ELCC
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

ELCC
Not Confirmed
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ELCC
Not Confirmed

HYDROCORTISONE; NEOMYCIN SULFATE

Brand Name : NEO-CORT-DOME

Dosage Form : CREAM;TOPICAL

Dosage Strength : 1%;EQ 3.5MG BASE/GM

Approval Date : 1984-06-05

Application Number : 50237

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

ELCC
Not Confirmed
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ELCC
Not Confirmed

HYDROCORTISONE; NEOMYCIN SULFATE

Brand Name : NEO-CORT-DOME

Dosage Form : CREAM;TOPICAL

Dosage Strength : 0.5%;EQ 3.5MG BASE/GM

Approval Date : 1984-06-05

Application Number : 50237

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

ELCC
Not Confirmed
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ELCC
Not Confirmed

ACETIC ACID, GLACIAL; HYDROCORTISONE; NEOMYCIN SULFATE

Brand Name : NEO-CORT-DOME

Dosage Form : SUSPENSION/DROPS;OTIC

Dosage Strength : 2%;1%;EQ 0.35% BASE

Approval Date : 1982-01-01

Application Number : 50238

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

ELCC
Not Confirmed
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ELCC
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

ELCC
Not Confirmed
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ELCC
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

ELCC
Not Confirmed
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ELCC
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

ELCC
Not Confirmed
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ELCC
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

ELCC
Not Confirmed
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ELCC
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**

Approval Date : 1985-08-09

Application Number : 50218

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

ELCC
Not Confirmed
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ELCC
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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