Bromday - 54868-6301-0 - (bromfenac)

Alphabetical Index


Drug Information of Bromday

Product NDC: 54868-6301
Proprietary Name: Bromday
Non Proprietary Name: bromfenac
Active Ingredient(s): .9    mg/mL & nbsp;   bromfenac
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Bromday

Product NDC: 54868-6301
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021664
Marketing Category: NDA
Start Marketing Date: 20110930

Package Information of Bromday

Package NDC: 54868-6301-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (54868-6301-0) > 1.7 mL in 1 BOTTLE, DROPPER

NDC Information of Bromday

NDC Code 54868-6301-0
Proprietary Name Bromday
Package Description 1 BOTTLE, DROPPER in 1 CARTON (54868-6301-0) > 1.7 mL in 1 BOTTLE, DROPPER
Product NDC 54868-6301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bromfenac
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20110930
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name BROMFENAC SODIUM
Strength Number .9
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Bromday


General Information