Prolensa - 24208-602-01 - (Bromfenac Sodium)

Alphabetical Index


Drug Information of Prolensa

Product NDC: 24208-602
Proprietary Name: Prolensa
Non Proprietary Name: Bromfenac Sodium
Active Ingredient(s): .7    mg/mL & nbsp;   Bromfenac Sodium
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Prolensa

Product NDC: 24208-602
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA203168
Marketing Category: NDA
Start Marketing Date: 20130408

Package Information of Prolensa

Package NDC: 24208-602-01
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-602-01) > 1.6 mL in 1 BOTTLE, DROPPER

NDC Information of Prolensa

NDC Code 24208-602-01
Proprietary Name Prolensa
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-602-01) > 1.6 mL in 1 BOTTLE, DROPPER
Product NDC 24208-602
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bromfenac Sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20130408
Marketing Category Name NDA
Labeler Name Bausch & Lomb Incorporated
Substance Name BROMFENAC SODIUM
Strength Number .7
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Prolensa


General Information