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Antabuse
Antabuse - 51285-524-02 - (Disulfiram)
Drug Information of Antabuse
| Product NDC: | 51285-524 |
| Proprietary Name: | Antabuse |
| Non Proprietary Name: | Disulfiram |
| Active Ingredient(s): | 500 mg/1 & nbsp; Disulfiram |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Antabuse
| Product NDC: | 51285-524 |
| Labeler Name: | Teva Women's Health, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088483 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060201 |
Package Information of Antabuse
| Package NDC: | 51285-524-02 |
| Package Description: | 100 TABLET in 1 BOTTLE (51285-524-02) |
NDC Information of Antabuse
| NDC Code | 51285-524-02 |
| Proprietary Name | Antabuse |
| Package Description | 100 TABLET in 1 BOTTLE (51285-524-02) |
| Product NDC | 51285-524 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Disulfiram |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060201 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Women's Health, Inc. |
| Substance Name | DISULFIRAM |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Acetyl Aldehyde Dehydrogenase Inhibitors [MoA],Aldehyde Dehydrogenase Inhibitor [EPC] |
