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Memantine Hydrochloride

NDC 29300-172, memantine hydrochloride, tablet, film coated, from Unichem Pharmaceuticals (USA), Inc..

Product NDC
29300-172
Status
Listed
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200022
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/29300-172 \
  -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
29300-172-0529300017205500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-172-05)
29300-172-162930001721660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-172-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff74edcb-d7ed-4b70-8f22-4cb5ccc58f90

  • NADAC price for package 29300017205

    GET /v1/drugs/nadac/29300017205

  • NADAC price for package 29300017216

    GET /v1/drugs/nadac/29300017216

Use it

Look up 29300-172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/29300-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 29300-172. 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.