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Memantine hydrochloride

NDC 53746-169, Memantine, tablet, film coated, from Amneal Pharmaceuticals of New York LLC.

Product NDC
53746-169
Status
Listed
Labeler
Amneal Pharmaceuticals of New York 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/53746-169 \
  -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
53746-169-10537460169101000 TABLET, FILM COATED in 1 BOTTLE (53746-169-10)
53746-169-305374601693030 TABLET, FILM COATED in 1 BOTTLE (53746-169-30)
53746-169-605374601696060 TABLET, FILM COATED in 1 BOTTLE (53746-169-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/054069b5-7aac-4106-821f-ebf7fd531b4f
  • NADAC price for package 53746016960

    GET /v1/drugs/nadac/53746016960

Use it

Look up 53746-169 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/53746-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 53746-169. 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.