| NDC Code | 62559-207-30 |
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| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-207-30) |
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| Product NDC | 62559-207 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Memantine And Donepezil Hydrochlorides |
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| Non-Proprietary Name | Memantine And Donepezil Hydrochlorides |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20250101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208237 |
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| Manufacturer | ANI Pharmaceuticals, Inc. |
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| Substance Name | DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE |
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| Strength | 10; 21 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA], N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA] |
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