Bromfenac - 54868-6343-0 - (Bromfenac sodium)

Alphabetical Index


Drug Information of Bromfenac

Product NDC: 54868-6343
Proprietary Name: Bromfenac
Non Proprietary Name: Bromfenac sodium
Active Ingredient(s): 1.035    mg/mL & nbsp;   Bromfenac sodium
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Bromfenac

Product NDC: 54868-6343
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201211
Marketing Category: ANDA
Start Marketing Date: 20120413

Package Information of Bromfenac

Package NDC: 54868-6343-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (54868-6343-0) > 2.5 mL in 1 BOTTLE, DROPPER

NDC Information of Bromfenac

NDC Code 54868-6343-0
Proprietary Name Bromfenac
Package Description 1 BOTTLE, DROPPER in 1 CARTON (54868-6343-0) > 2.5 mL in 1 BOTTLE, DROPPER
Product NDC 54868-6343
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bromfenac sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20120413
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name BROMFENAC SODIUM
Strength Number 1.035
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Bromfenac


General Information