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Flurbiprofen - 63629-1250-1 - (Flurbiprofen)

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Drug Information of Flurbiprofen

Product NDC: 63629-1250
Proprietary Name: Flurbiprofen
Non Proprietary Name: Flurbiprofen
Active Ingredient(s): 100    mg/1 & nbsp;   Flurbiprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Flurbiprofen

Product NDC: 63629-1250
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074431
Marketing Category: ANDA
Start Marketing Date: 19950602

Package Information of Flurbiprofen

Package NDC: 63629-1250-1
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (63629-1250-1)

NDC Information of Flurbiprofen

NDC Code 63629-1250-1
Proprietary Name Flurbiprofen
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (63629-1250-1)
Product NDC 63629-1250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flurbiprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950602
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name FLURBIPROFEN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Flurbiprofen


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