| NDC Code | 68462-136-10 |
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| Package Description | 1000 TABLET in 1 BOTTLE (68462-136-10) |
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| Product NDC | 68462-136 |
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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 | 20070702 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078157 |
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| Manufacturer | Glenmark Generics Inc., USA |
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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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