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    01

    Alembic Pharmaceuticals Limited

    India
    AACR Annual meeting
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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

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    Approval Date : 2019-06-21

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    Alembic Pharmaceuticals Limited

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    Brand Name : BROMFENAC SODIUM

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    Dosage Strength : EQ 0.07% ACID

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    Approval Date : 2024-07-08

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    03

    Amneal Pharmaceuticals

    U.S.A
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    Dosage Strength : EQ 0.07% ACID

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    Approval Date : 2024-07-29

    Application Number : 210962

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    Amring Pharma

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

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    Dosage Strength : EQ 0.09% ACID

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    Approval Date : 2013-01-09

    Application Number : 202030

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    05

    Apotex Inc

    Canada
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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

    Packaging :

    Approval Date : 2014-06-19

    Application Number : 202435

    Regulatory Info : DISCN

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    06

    Apotex Inc

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

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    Approval Date : 2014-06-23

    Application Number : 202620

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    07

    Apotex Inc

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.07% ACID

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    Approval Date : 2024-07-08

    Application Number : 207334

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    Aurobindo Pharma Limited

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

    Packaging :

    Approval Date : 2022-03-18

    Application Number : 204813

    Regulatory Info : RX

    Registration Country : USA

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    09

    Bausch & Lomb Incorporated

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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**

    Packaging :

    Approval Date : 2005-03-24

    Application Number : 21664

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Bausch & Lomb Incorporated

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    AACR Annual meeting
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    Regulatory Info : DISCN

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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**

    Packaging :

    Approval Date : 2010-10-16

    Application Number : 21664

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Bausch & Lomb Incorporated

    Canada
    AACR Annual meeting
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    BROMFENAC SODIUM

    Brand Name : PROLENSA

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.07% ACID

    Packaging :

    Approval Date : 2013-04-05

    Application Number : 203168

    Regulatory Info : RX

    Registration Country : USA

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    12

    Chartwell Pharmaceuticals llc

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Chartwell Pharmaceuticals llc

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    Regulatory Info : DISCN

    Registration Country : USA

    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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    13

    COASTAL PHARMS

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    14

    Freedom Biopharma

    India
    AACR Annual meeting
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    Freedom Biopharma

    India
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    Registration Country : India

    Bromfenac Sodium; Benzalkonium Chloride

    Brand Name : FREEDOM B-FENAC- Eye drop 5ML

    Dosage Form : Eye drop

    Dosage Strength : 0.09%; 0.02%

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    Approval Date :

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    Registration Country : India

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    15

    GLAND PHARMA LIMITED

    India
    AACR Annual meeting
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    Regulatory Info : RX

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

    Packaging :

    Approval Date : 2020-03-17

    Application Number : 211029

    Regulatory Info : RX

    Registration Country : USA

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    16

    Indoco Remedies Limited

    India
    AACR Annual meeting
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    Regulatory Info : Generic

    Registration Country : India

    Bromfenac Sodium

    Brand Name :

    Dosage Form : Ophthalmic Solution

    Dosage Strength : 0.9%

    Packaging : 1.7 ml

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : India

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    17

    Lupin Ltd

    India
    AACR Annual meeting
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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.09% ACID

    Packaging :

    Approval Date : 2023-08-15

    Application Number : 202903

    Regulatory Info : RX

    Registration Country : USA

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    18

    Lupin Ltd

    India
    AACR Annual meeting
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    Lupin Ltd

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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.07% ACID

    Packaging :

    Approval Date : 2023-11-22

    Application Number : 206027

    Regulatory Info : RX

    Registration Country : USA

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    19

    Lupin Ltd

    India
    AACR Annual meeting
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    BROMFENAC SODIUM

    Brand Name : BROMFENAC SODIUM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.075% ACID

    Packaging :

    Approval Date : 2024-02-02

    Application Number : 211239

    Regulatory Info : RX

    Registration Country : USA

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    Rising Pharmaceuticals Inc

    U.S.A
    AACR Annual meeting
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    Regulatory Info : DISCN

    Registration Country : USA

    BROMFENAC SODIUM

    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

    Registration Country : USA

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    21

    Sentiss Pharma

    India
    AACR Annual meeting
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    India
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    Regulatory Info : RX

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    BROMFENAC SODIUM

    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

    Registration Country : USA

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    22

    Sun Pharmaceutical Industries Limit...

    India
    AACR Annual meeting
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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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    23

    Pharma Swiss Ceska republika sro

    Country
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    Regulatory Info :

    Registration Country : Sweden

    bromfenaknatrium

    Brand Name : Yellox

    Dosage Form : EYE DROPS, SOLUTION

    Dosage Strength : 0.9 MG / ML

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Sweden

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