Antabuse - 54868-5034-1 - (Disulfiram)

Alphabetical Index


Drug Information of Antabuse

Product NDC: 54868-5034
Proprietary Name: Antabuse
Non Proprietary Name: Disulfiram
Active Ingredient(s): 250    mg/1 & nbsp;   Disulfiram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Antabuse

Product NDC: 54868-5034
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088482
Marketing Category: ANDA
Start Marketing Date: 20040330

Package Information of Antabuse

Package NDC: 54868-5034-1
Package Description: 30 TABLET in 1 BOTTLE (54868-5034-1)

NDC Information of Antabuse

NDC Code 54868-5034-1
Proprietary Name Antabuse
Package Description 30 TABLET in 1 BOTTLE (54868-5034-1)
Product NDC 54868-5034
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Disulfiram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040330
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name DISULFIRAM
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Acetyl Aldehyde Dehydrogenase Inhibitors [MoA],Aldehyde Dehydrogenase Inhibitor [EPC]

Complete Information of Antabuse


General Information