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Memantine Hydrochloride

NDC 27241-071, Memantine Hydrochloride, tablet, from Ajanta Pharma USA Inc..

Product NDC
27241-071
Status
Listed
Labeler
Ajanta Pharma USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206528
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/27241-071 \
  -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
27241-071-0527241007105500 TABLET in 1 BOTTLE (27241-071-05)
27241-071-062724100710660 TABLET in 1 BOTTLE (27241-071-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/292671f2-f221-4a3d-a110-a266a9527e04

  • NADAC price for package 27241007105

    GET /v1/drugs/nadac/27241007105

  • NADAC price for package 27241007106

    GET /v1/drugs/nadac/27241007106

Use it

Look up 27241-071 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/27241-071 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 27241-071. 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.