Product NDC: | 0603-3433 |
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) |
Product NDC: | 0603-3433 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091563 |
Marketing Category: | ANDA |
Start Marketing Date: | 20121231 |
Package NDC: | 0603-3433-21 |
Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0603-3433-21) |
NDC Code | 0603-3433-21 |
Proprietary Name | Disulfiram |
Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0603-3433-21) |
Product NDC | 0603-3433 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | disulfiram |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20121231 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | DISULFIRAM |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Acetyl Aldehyde Dehydrogenase Inhibitors [MoA],Aldehyde Dehydrogenase Inhibitor [EPC] |