| NDC Code | 0115-1911-02 |
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| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0115-1911-02) |
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| Product NDC | 0115-1911 |
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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 | 20211116 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076132 |
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| Manufacturer | Amneal Pharmaceuticals of New York LLC |
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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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