| NDC Code | 55111-250-79 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (55111-250-79) / 10 TABLET in 1 BLISTER PACK (55111-250-78) |
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| Product NDC | 55111-250 |
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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 | ANDA076390 |
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| Manufacturer | Dr.Reddys Laboratories Limited |
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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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