| NDC Code | 16571-852-03 |
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| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-852-03) |
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| Product NDC | 16571-852 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Memantine Hydrochloride |
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| Non-Proprietary Name | Memantine |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20250418 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA206032 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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| Substance Name | MEMANTINE HYDROCHLORIDE |
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| Strength | 7 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA] |
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