Memantine Hydrochloride
NDC 72162-2003, Memantine Hydrochloride, tablet, from Bryant Ranch Prepack.
- Product NDC
- 72162-2003
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090961
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2003 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MEMANTINE HYDROCHLORIDE5 mg/1
Pharmacologic classes
N-methyl-D-aspartate Receptor Antagonist [EPC]; NMDA Receptor Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-2003-5 | 72162200305 | 500 TABLET in 1 BOTTLE (72162-2003-5) |
| 72162-2003-6 | 72162200306 | 60 TABLET in 1 BOTTLE (72162-2003-6) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/0ad2246a-ffa0-43a0-8094-58279d3e3a74
Use it
Look up 72162-2003 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2003 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-2003. 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.