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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

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PharmaCompass

01

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

BROMFENAC SODIUM

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

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02

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

BROMFENAC SODIUM

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

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03

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

BROMFENAC SODIUM

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

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04

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

BROMFENAC SODIUM

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

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05

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

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

Registration Country : USA

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06

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

BROMFENAC SODIUM

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

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07

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

BROMFENAC SODIUM

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

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08

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

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

PackExpo
Not Confirmed
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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

PackExpo
Not Confirmed
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PackExpo
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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

PackExpo
Not Confirmed
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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

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

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

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

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

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

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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15

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

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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16

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

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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17

PackExpo
Not Confirmed
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PackExpo
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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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18

PackExpo
Not Confirmed
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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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19

PackExpo
Not Confirmed
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PackExpo
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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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20

PackExpo
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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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