Disulfiram - 0093-5035-01 - (Disulfiram)

Alphabetical Index


Drug Information of Disulfiram

Product NDC: 0093-5035
Proprietary Name: Disulfiram
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 Disulfiram

Product NDC: 0093-5035
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088482
Marketing Category: ANDA
Start Marketing Date: 20110415

Package Information of Disulfiram

Package NDC: 0093-5035-01
Package Description: 100 TABLET in 1 BOTTLE (0093-5035-01)

NDC Information of Disulfiram

NDC Code 0093-5035-01
Proprietary Name Disulfiram
Package Description 100 TABLET in 1 BOTTLE (0093-5035-01)
Product NDC 0093-5035
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Disulfiram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110415
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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 Disulfiram


General Information