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01 2Alembic Pharmaceuticals Limited
02 1Amneal Pharmaceuticals
03 1Amring Pharma
04 3Apotex Inc
05 1Aurobindo Pharma Limited
06 6Bausch & Lomb Incorporated
07 1COASTAL PHARMS
08 1Chartwell Pharmaceuticals llc
09 2Croma-Pharma
10 1Freedom Biopharma
11 1GLAND PHARMA LIMITED
12 1Indoco Remedies Limited
13 3Lupin Ltd
14 1Pharmaswiss Ceska Republika Sro
15 1Rising Pharmaceuticals Inc
16 1Sentiss Pharma
17 1Sun Pharmaceutical Industries Limited
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01 6Eye Drop Solution
02 1Eye drop
03 1Ophthalmic Solution
04 20SOLUTION/DROPS;OPHTHALMIC
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01 5Authorized
02 1Cancelled
03 8DISCN
04 1Generic
05 12RX
06 1Blank
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01 1BROMDAY
02 16BROMFENAC SODIUM
03 1BROMSITE
04 1FREEDOM B-FENAC- Eye drop 5ML
05 1PROLENSA
06 1XIBROM
07 6Yellox
08 1Blank
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01 2India
02 6Spain
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