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01 2ALEMBIC

02 1AMNEAL

03 1AMRING PHARMS

04 3APOTEX

05 1BAUSCH AND LOMB

06 2BAUSCH AND LOMB INC

07 1CHARTWELL RX

08 1COASTAL PHARMS

09 1EUGIA PHARMA

10 1GLAND PHARMA LTD

11 3LUPIN LTD

12 1RISING

13 1SENTISS

14 1SUN PHARM

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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BROMFENAC SODIUM

Brand Name : BROMFENAC SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.09% ACID

Approval Date : 2013-01-09

Application Number : 202030

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BROMFENAC SODIUM

Brand Name : BROMFENAC SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.09% ACID

Approval Date : 2014-06-19

Application Number : 202435

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BROMFENAC SODIUM

Brand Name : BROMFENAC SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.09% ACID

Approval Date : 2014-06-23

Application Number : 202620

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

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Dosage Strength : EQ 0.09% ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2005-03-24

Application Number : 21664

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

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Dosage Strength : EQ 0.09% ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2010-10-16

Application Number : 21664

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BROMFENAC SODIUM

Brand Name : PROLENSA

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.07% ACID

Approval Date : 2013-04-05

Application Number : 203168

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BROMFENAC SODIUM

Brand Name : BROMFENAC SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.09% ACID

Approval Date : 2015-02-10

Application Number : 201941

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BROMFENAC SODIUM

Brand Name : BROMFENAC SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.09% ACID

Approval Date : 2011-05-11

Application Number : 201211

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BROMFENAC SODIUM

Brand Name : BROMFENAC SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.09% ACID

Approval Date : 2023-08-15

Application Number : 202903

RX/OTC/DISCN : RX

RLD : No

TE Code : AT2

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BROMFENAC SODIUM

Brand Name : BROMFENAC SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.09% ACID

Approval Date : 2019-06-03

Application Number : 203368

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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