01 2Alembic Pharmaceuticals Limited
02 1Amneal Pharmaceuticals
03 1Amring Pharma
04 3Apotex Inc
05 1Aurobindo Pharma Limited
06 3Bausch & Lomb Incorporated
07 1COASTAL PHARMS
08 1Chartwell Pharmaceuticals llc
09 1GLAND PHARMA LIMITED
10 1Indoco Remedies Limited
11 3Lupin Ltd
12 1Pharma Swiss Ceska republika sro
13 1Rising Pharmaceuticals Inc
14 1Sentiss Pharma
15 1Sun Pharmaceutical Industries Limited
01 1EYE DROPS, SOLUTION
02 1Ophthalmic Solution
03 20SOLUTION/DROPS;OPHTHALMIC
01 8DISCN
02 1Generic
03 12RX
04 1Blank
01 1BROMDAY
02 16BROMFENAC SODIUM
03 1BROMSITE
04 1PROLENSA
05 1XIBROM
06 1Yellox
07 1Blank
01 1India
02 1Sweden
03 20USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BROMFENAC SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.09% ACID
Packaging :
Approval Date : 2019-06-21
Application Number : 210560
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BROMFENAC SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.07% ACID
Packaging :
Approval Date : 2024-07-08
Application Number : 214340
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BROMFENAC SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.07% ACID
Packaging :
Approval Date : 2024-07-29
Application Number : 210962
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BROMFENAC SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.09% ACID
Packaging :
Approval Date : 2013-01-09
Application Number : 202030
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BROMFENAC SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.09% ACID
Packaging :
Approval Date : 2014-06-23
Application Number : 202620
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BROMFENAC SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.07% ACID
Packaging :
Approval Date : 2024-07-08
Application Number : 207334
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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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