Memantine Hydrochloride
NDC 50268-588, memantine hydrochloride, tablet, film coated, from AvPAK.
- Product NDC
- 50268-588
- Status
- Listed
- Labeler
- AvPAK
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA200022
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50268-588 \ -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 |
|---|---|---|
| 50268-588-13 | 50268058813 | 30 BLISTER PACK in 1 BOX (50268-588-13) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-588-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/11d27c75-fdc0-f9da-e063-6394a90ac6b0NADAC price for package 50268058813
GET /v1/drugs/nadac/50268058813
Use it
Look up 50268-588 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50268-588 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50268-588. 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.