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memantine hydrochloride

NDC 65162-169, memantine, tablet, film coated, from Amneal Pharmaceuticals LLC.

Product NDC
65162-169
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090041
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-169 \
  -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 NDCNDC-11Package
65162-169-066516201690660 TABLET, FILM COATED in 1 BOTTLE (65162-169-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f73e0df0-4af4-42f1-bde6-3cccb47ca378

  • NADAC price for package 65162016906

    GET /v1/drugs/nadac/65162016906

Use it

Look up 65162-169 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-169. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.