Diflunisal - 54868-3049-4 - (Diflunisal)

Alphabetical Index


Drug Information of Diflunisal

Product NDC: 54868-3049
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: 54868-3049
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073673
Marketing Category: ANDA
Start Marketing Date: 20090721

Package Information of Diflunisal

Package NDC: 54868-3049-4
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (54868-3049-4)

NDC Information of Diflunisal

NDC Code 54868-3049-4
Proprietary Name Diflunisal
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (54868-3049-4)
Product NDC 54868-3049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diflunisal
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090721
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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