Bromday - 67425-999-34 - (bromfenac)

Alphabetical Index


Drug Information of Bromday

Product NDC: 67425-999
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: 67425-999
Labeler Name: Ista Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021664
Marketing Category: NDA
Start Marketing Date: 20100920

Package Information of Bromday

Package NDC: 67425-999-34
Package Description: 2 BOTTLE, DROPPER in 1 CARTON (67425-999-34) > 1.7 mL in 1 BOTTLE, DROPPER

NDC Information of Bromday

NDC Code 67425-999-34
Proprietary Name Bromday
Package Description 2 BOTTLE, DROPPER in 1 CARTON (67425-999-34) > 1.7 mL in 1 BOTTLE, DROPPER
Product NDC 67425-999
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bromfenac
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20100920
Marketing Category Name NDA
Labeler Name Ista Pharmaceuticals, 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