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    01 2Alembic Pharmaceuticals Limited

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    Alembic Pharmaceuticals Limited

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

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    Approval Date : 2019-06-21

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

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    Approval Date : 2024-07-08

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    BROMFENAC SODIUM

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    Approval Date : 2024-07-29

    Application Number : 210962

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    Brand Name : BROMFENAC SODIUM

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    Approval Date : 2013-01-09

    Application Number : 202030

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

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    Approval Date : 2014-06-19

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

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    Approval Date : 2014-06-23

    Application Number : 202620

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    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

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    Approval Date : 2024-07-08

    Application Number : 207334

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    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

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    Approval Date : 2022-03-18

    Application Number : 204813

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    BROMFENAC SODIUM

    Brand Name : XIBROM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2005-03-24

    Application Number : 21664

    Regulatory Info : DISCN

    Registration Country : USA

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    10

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    BROMFENAC SODIUM

    Brand Name : BROMDAY

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2010-10-16

    Application Number : 21664

    Regulatory Info : DISCN

    Registration Country : USA

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    BROMFENAC SODIUM

    Brand Name : PROLENSA

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.07% ACID

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    Approval Date : 2013-04-05

    Application Number : 203168

    Regulatory Info : RX

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    12

    Chartwell Pharmaceuticals llc

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

    Packaging :

    Approval Date : 2015-02-10

    Application Number : 201941

    Regulatory Info : DISCN

    Registration Country : USA

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    COASTAL PHARMS

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

    Packaging :

    Approval Date : 2011-05-11

    Application Number : 201211

    Regulatory Info : DISCN

    Registration Country : USA

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    GLAND PHARMA LIMITED

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    GLAND PHARMA LIMITED

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    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

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    Approval Date : 2020-03-17

    Application Number : 211029

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    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

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    Approval Date : 2023-08-15

    Application Number : 202903

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    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.07% ACID

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    Approval Date : 2023-11-22

    Application Number : 206027

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    Lupin Ltd

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    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.075% ACID

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    Approval Date : 2024-02-02

    Application Number : 211239

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    Rising Pharmaceuticals Inc

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    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

    Packaging :

    Approval Date : 2019-06-03

    Application Number : 203368

    Regulatory Info : DISCN

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    Sentiss Pharma

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    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

    Packaging :

    Approval Date : 2014-01-22

    Application Number : 203395

    Regulatory Info : RX

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    Sun Pharmaceutical Industries Limit...

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    BROMFENAC SODIUM

    Brand Name : BROMSITE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.075% ACID

    Packaging :

    Approval Date : 2016-04-08

    Application Number : 206911

    Regulatory Info : RX

    Registration Country : USA

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