| NDC Code | 0093-7294-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (0093-7294-01) |
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| Product NDC | 0093-7294 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Terbinafine Hydrochloride |
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| Non-Proprietary Name | Terbinafine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20070703 |
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| End Marketing Date | 20140228 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076377 |
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| Manufacturer | Teva Pharmaceuticals USA Inc |
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| Substance Name | TERBINAFINE HYDROCHLORIDE |
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| Strength | 250 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |
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