Diflunisal - 0093-0755-05 - (Diflunisal)

Alphabetical Index


Drug Information of Diflunisal

Product NDC: 0093-0755
Proprietary Name: Diflunisal
Non Proprietary Name: Diflunisal
Active Ingredient(s): 500    mg/1 & nbsp;   Diflunisal
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diflunisal

Product NDC: 0093-0755
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073673
Marketing Category: ANDA
Start Marketing Date: 19921101

Package Information of Diflunisal

Package NDC: 0093-0755-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0093-0755-05)

NDC Information of Diflunisal

NDC Code 0093-0755-05
Proprietary Name Diflunisal
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0093-0755-05)
Product NDC 0093-0755
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diflunisal
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19921101
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name DIFLUNISAL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Diflunisal


General Information