OCUFEN - 54868-1158-0 - (flurbiprofen sodium)

Alphabetical Index


Drug Information of OCUFEN

Product NDC: 54868-1158
Proprietary Name: OCUFEN
Non Proprietary Name: flurbiprofen sodium
Active Ingredient(s): .3    mg/mL & nbsp;   flurbiprofen sodium
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of OCUFEN

Product NDC: 54868-1158
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019404
Marketing Category: NDA
Start Marketing Date: 19940428

Package Information of OCUFEN

Package NDC: 54868-1158-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (54868-1158-0) > 2.5 mL in 1 BOTTLE, DROPPER

NDC Information of OCUFEN

NDC Code 54868-1158-0
Proprietary Name OCUFEN
Package Description 1 BOTTLE, DROPPER in 1 CARTON (54868-1158-0) > 2.5 mL in 1 BOTTLE, DROPPER
Product NDC 54868-1158
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name flurbiprofen sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19940428
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name FLURBIPROFEN SODIUM
Strength Number .3
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of OCUFEN


General Information