memantine hydrochloride
NDC 71610-011, memantine hydrochloride, tablet, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-011
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA021487
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71610-011 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MEMANTINE HYDROCHLORIDE10 mg/1
Pharmacologic classes
N-methyl-D-aspartate Receptor Antagonist [EPC]; NMDA Receptor Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71610-011-18 | 71610001118 | 3000 TABLET in 1 BOTTLE (71610-011-18) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c8f5c20b-4573-44c5-89fc-4da11b2e1fe1
Use it
Look up 71610-011 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-011 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-011. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.