| NDC Code | 51655-364-26 |
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| Package Description | 90 TABLET in 1 BOTTLE (51655-364-26) |
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| Product NDC | 51655-364 |
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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 | 20200528 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077714 |
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| Manufacturer | Northwind Pharmaceuticals, LLC |
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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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