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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.

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    LEBSA- Your strategic API source for niche molecules.

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    Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.

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    Sulfacetamide Sodium

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    Approval Date : 1989-09-29

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    PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

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    Approval Date : 1996-12-23

    Application Number : 19931

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    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

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    Approval Date : 1994-12-28

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    PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.23% PHOSPHATE;10%

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    Approval Date : 1995-12-29

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    Bayer AG

    Germany
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    SULFACETAMIDE SODIUM

    Brand Name : SODIUM SULAMYD

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

    Application Number : 5963

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    Bayer AG

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    SULFACETAMIDE SODIUM

    Brand Name : SODIUM SULAMYD

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

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    Bayer AG

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    SULFACETAMIDE SODIUM

    Brand Name : SODIUM SULAMYD

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 30% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

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    PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

    Brand Name : METIMYD

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.5%;10%

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    Approval Date : 1982-01-01

    Application Number : 10210

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    Bayer AG

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    Brand Name : METIMYD

    Dosage Form : OINTMENT;OPHTHALMIC

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    Approval Date : 1984-09-09

    Application Number : 10210

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    Epic Pharma. LLC.

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    SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 30%

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    Approval Date : 1999-05-25

    Application Number : 40216

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    Epic Pharma. LLC.

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    PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

    Brand Name : SULSTER

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.23% PHOSPHATE;10%

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    Approval Date : 1996-07-30

    Application Number : 74511

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    Epic Pharma. LLC.

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    SULFACETAMIDE SODIUM

    Brand Name : SODIUM SULFACETAMIDE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10%

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    Approval Date : 1982-01-01

    Application Number : 83021

    Regulatory Info : DISCN

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    Fougera Pharmaceuticals Inc.

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    SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 10%

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    Approval Date : 2006-11-17

    Application Number : 77015

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    Genus Lifesciences

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    PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.23% PHOSPHATE;10%

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    Approval Date : 1993-05-27

    Application Number : 73630

    Regulatory Info : DISCN

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    Novartis Pharmaceuticals Corporatio...

    Switzerland
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    Switzerland
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    PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

    Brand Name : VASOCIDIN

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.23% PHOSPHATE;10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1988-08-26

    Application Number : 18988

    Regulatory Info : DISCN

    Registration Country : USA

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    Novartis Pharmaceuticals Corporatio...

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    SULFACETAMIDE SODIUM

    Brand Name : SULF-10

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 80025

    Regulatory Info : DISCN

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    Israel
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    Regulatory Info : RX

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 10%

    Packaging :

    Approval Date : 2009-03-23

    Application Number : 78649

    Regulatory Info : RX

    Registration Country : USA

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    25

    Padagis

    Israel
    Duphat
    Not Confirmed
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    Padagis

    Israel
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    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 80029

    Regulatory Info : RX

    Registration Country : USA

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    26

    ScieGen Pharmaceuticals

    U.S.A
    Duphat
    Not Confirmed
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    ScieGen Pharmaceuticals

    U.S.A
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10%

    Packaging :

    Approval Date : 1999-05-25

    Application Number : 40215

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    Taro Pharmaceutical Industries

    U.S.A
    Duphat
    Not Confirmed
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    Taro Pharmaceutical Industries

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 10%

    Packaging :

    Approval Date : 2009-05-20

    Application Number : 78668

    Regulatory Info : RX

    Registration Country : USA

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    28

    OPTOPICS

    Country
    Duphat
    Not Confirmed
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    OPTOPICS

    Country
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : SULFACEL-15

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 15%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 80024

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    MIZA PHARMS USA

    Country
    Duphat
    Not Confirmed
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    MIZA PHARMS USA

    Country
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    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : OCUSULF-10

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 80660

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    MIZA PHARMS USA

    Country
    Duphat
    Not Confirmed
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    MIZA PHARMS USA

    Country
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    Duphat
    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : OCUSULF-30

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 30%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 80660

    Regulatory Info : DISCN

    Registration Country : USA

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