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    Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.

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    01

    AbbVie Inc

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    Regulatory Info : Originator

    Registration Country : South Africa

    Neomycin sulphate

    Brand Name : FML Neo Liquifilm Ophthalmic Suspension

    Dosage Form : OPD

    Dosage Strength : 5mg/ml

    Packaging : 5X1mg/ml

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    Registration Country : South Africa

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    Allergan Aesthetics

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    Regulatory Info : DISCN

    Registration Country : USA

    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

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    03

    Alcon Inc

    U.S.A
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    Alcon Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : STATROL

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : EQ 3.5MG BASE/GM;10,000 UNITS/GM

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    Approval Date : 1982-01-01

    Application Number : 50344

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE; NEOMYCIN SULFATE

    Brand Name : NEO-CORT-DOME

    Dosage Form : CREAM;TOPICAL

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

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    Approval Date : 1984-06-05

    Application Number : 50237

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE; NEOMYCIN SULFATE

    Brand Name : NEO-CORT-DOME

    Dosage Form : CREAM;TOPICAL

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

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    Approval Date : 1984-06-05

    Application Number : 50237

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    ACETIC ACID, GLACIAL; HYDROCORTISONE; NEOMYCIN SULFATE

    Brand Name : NEO-CORT-DOME

    Dosage Form : SUSPENSION/DROPS;OTIC

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

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    Approval Date : 1982-01-01

    Application Number : 50238

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    DELCOR ASSET

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    Regulatory Info : DISCN

    Registration Country : USA

    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

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    08

    Eli Lilly

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    Regulatory Info : DISCN

    Registration Country : USA

    FLURANDRENOLIDE; NEOMYCIN SULFATE

    Brand Name : CORDRAN N

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50345

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Eli Lilly

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    Regulatory Info : DISCN

    Registration Country : USA

    FLURANDRENOLIDE; NEOMYCIN SULFATE

    Brand Name : CORDRAN N

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50346

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    GSK

    United Kingdom
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    GSK

    United Kingdom
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    Regulatory Info : DISCN

    Registration Country : USA

    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

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    11

    Harrow

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    Harrow

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    Regulatory Info : RX

    Registration Country : USA

    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

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    12

    Merck & Co

    U.S.A
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

    Brand Name : NEODECADRON

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50322

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

    Brand Name : NEODECADRON

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50324

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Merck & Co

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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE; PREDNISOLONE SODIUM PHOSPHATE

    Brand Name : NEO-HYDELTRASOL

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : EQ 3.5MG BASE/GM;EQ 0.25% PHOSPHATE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50378

    Regulatory Info : DISCN

    Registration Country : USA

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    Pfizer Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    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

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    16

    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    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

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    17

    Pfizer Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    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

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    18

    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE

    Brand Name : MYCIFRADIN

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 87.5MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50285

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Sandoz B2B

    Switzerland
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    Switzerland
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    Regulatory Info : RX

    Registration Country : USA

    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

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    20

    PH HEALTH

    Country
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    Regulatory Info : RX

    Registration Country : USA

    COLISTIN SULFATE; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; THONZONIUM BROMIDE

    Brand Name : COLY-MYCIN S

    Dosage Form : SUSPENSION/DROPS;OTIC

    Dosage Strength : EQ 3MG BASE/ML;10MG/ML;EQ 3.3MG BASE/ML;0.5MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50356

    Regulatory Info : RX

    Registration Country : USA

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