| NDC Code | 16571-855-09 |
|---|
| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-855-09) |
|---|
| Product NDC | 16571-855 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Memantine Hydrochloride |
|---|
| Non-Proprietary Name | Memantine |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20250601 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA206032 |
|---|
| Manufacturer | Rising Pharma Holdings, Inc. |
|---|
| Substance Name | MEMANTINE HYDROCHLORIDE |
|---|
| Strength | 28 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA] |
|---|