| NDC Code | 51672-2083-8 |
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| Package Description | 1 TUBE in 1 CARTON (51672-2083-8) > 12 g in 1 TUBE |
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| Product NDC | 51672-2083 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Terbinafine Hydrochloride |
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| Non-Proprietary Name | Terbinafine Hydrochloride |
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| Dosage Form | CREAM |
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| Usage | TOPICAL |
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| Start Marketing Date | 20070702 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077511 |
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| Manufacturer | Taro Pharmaceuticals U.S.A., Inc. |
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| Substance Name | TERBINAFINE HYDROCHLORIDE |
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| Strength | 1 |
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| Strength Unit | g/100g |
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| Pharmacy Classes | Allylamine Antifungal [EPC], Allylamine [CS] |
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