Memantine Hydrochloride
NDC 0832-1113, Memantine Hydrochloride, tablet, film coated, from Upsher-Smith Laboratories, LLC.
- Product NDC
- 0832-1113
- Status
- Listed
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090043
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0832-1113 \ -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 |
|---|---|---|
| 0832-1113-60 | 00832111360 | 60 TABLET, FILM COATED in 1 BOTTLE (0832-1113-60) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6e0ade9e-b721-4701-bcb7-de464e19e707NADAC price for package 00832111360
GET /v1/drugs/nadac/00832111360
Use it
Look up 0832-1113 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0832-1113 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0832-1113. 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.