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    Gangwal Healthcare is powered by innovation, driving health, wellness & healing.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    Sulfacetamide Sodium

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    01 6Allergan Aesthetics

    02 1Taro Pharmaceutical Industries

    03 5Alcon Inc

    04 13Bausch & Lomb Incorporated

    05 5Bayer AG

    06 6Epic Pharma. LLC.

    07 2Farmak JSC

    08 1Fougera Pharmaceuticals Inc.

    09 1Genus Lifesciences

    10 2MIZA PHARMS USA

    11 4Novartis Pharmaceuticals Corporation

    12 1OPTOPICS

    13 2Padagis

    14 2Pharmascience Inc.

    15 4SOLA BARNES HIND

    16 1Sandoz B2B

    17 1ScieGen Pharmaceuticals

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    01

    Allergan Aesthetics

    U.S.A
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    The Pharmacy Technology
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    Regulatory Info : DISCN

    Registration Country : USA

    PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

    Brand Name : BLEPHAMIDE

    Dosage Form : SUSPENSION;OPHTHALMIC

    Dosage Strength : 0.2%;10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12813

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Allergan Aesthetics

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    FLUOROMETHOLONE; SULFACETAMIDE SODIUM

    Brand Name : FML-S

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.1%;10%

    Packaging :

    Approval Date : 1989-09-29

    Application Number : 19525

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Allergan Aesthetics

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : BLEPH-10

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 80028

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Allergan Aesthetics

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : BLEPH-30

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 30%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 80028

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Allergan Aesthetics

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : BLEPH-10

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84015

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Allergan Aesthetics

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

    Brand Name : BLEPHAMIDE S.O.P.

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 0.2%;10%

    Packaging :

    Approval Date : 1986-12-03

    Application Number : 87748

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    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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    08

    Bausch & Lomb Incorporated

    Canada
    The Pharmacy Technology
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    Bausch & Lomb Incorporated

    Canada
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    Regulatory Info : RX

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : KLARON

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 10%

    Packaging :

    Approval Date : 1996-12-23

    Application Number : 19931

    Regulatory Info : RX

    Registration Country : USA

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    09

    Bausch & Lomb Incorporated

    Canada
    The Pharmacy Technology
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    Bausch & Lomb Incorporated

    Canada
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    Regulatory Info : RX

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10%

    Packaging :

    Approval Date : 1994-12-28

    Application Number : 40066

    Regulatory Info : RX

    Registration Country : USA

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    10

    Bausch & Lomb Incorporated

    Canada
    The Pharmacy Technology
    Not Confirmed
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    Bausch & Lomb Incorporated

    Canada
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    The Pharmacy Technology
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    Regulatory Info : RX

    Registration Country : USA

    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%

    Packaging :

    Approval Date : 1995-12-29

    Application Number : 74449

    Regulatory Info : RX

    Registration Country : USA

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    11

    Bayer AG

    Germany
    The Pharmacy Technology
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    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 5963

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Bayer AG

    Germany
    The Pharmacy Technology
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    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 5963

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Bayer AG

    Germany
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    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 5963

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

    Brand Name : METIMYD

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.5%;10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 10210

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Bayer AG

    Germany
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    Regulatory Info : DISCN

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    PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

    Brand Name : METIMYD

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 0.5%;10%

    Packaging :

    Approval Date : 1984-09-09

    Application Number : 10210

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Epic Pharma. LLC.

    U.S.A
    The Pharmacy Technology
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    Epic Pharma. LLC.

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFACETAMIDE SODIUM

    Brand Name : SULFACETAMIDE SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 30%

    Packaging :

    Approval Date : 1999-05-25

    Application Number : 40216

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Epic Pharma. LLC.

    U.S.A
    The Pharmacy Technology
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

    Brand Name : SULSTER

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.23% PHOSPHATE;10%

    Packaging :

    Approval Date : 1996-07-30

    Application Number : 74511

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Genus Lifesciences

    U.S.A
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    Genus Lifesciences

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    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%

    Packaging :

    Approval Date : 1993-05-27

    Application Number : 73630

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Novartis Pharmaceuticals Corporatio...

    Switzerland
    The Pharmacy Technology
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    Switzerland
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1988-08-26

    Application Number : 18988

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    ScieGen Pharmaceuticals

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    ScieGen Pharmaceuticals

    U.S.A
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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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