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Disulfiram
Disulfiram - 0093-5035-01 - (Disulfiram)
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] |
