| NDC Code | 70934-947-45 |
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| Package Description | 45 TABLET in 1 BOTTLE, PLASTIC (70934-947-45) |
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| Product NDC | 70934-947 |
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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 | 20220203 |
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| End Marketing Date | 20240331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077714 |
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| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
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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 Antifungal [EPC], Allylamine [CS] |
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