| NDC Code | 52959-305-30 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (52959-305-30) |
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| Product NDC | 52959-305 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Rimantadine Hydrochloride |
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| Non-Proprietary Name | Rimantadine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20050401 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076132 |
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| Manufacturer | H.J. Harkins Company, Inc. |
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| Substance Name | RIMANTADINE HYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |
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