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Memantine hydrochloride

NDC 68180-230, Memantine hydrochloride, tablet, film coated, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-230
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090051
DEA schedule
None
Request
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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
68180-230-076818002300760 TABLET, FILM COATED in 1 BOTTLE (68180-230-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b4a0162-9cb4-4ba6-8c02-95c2955734ae

  • NADAC price for package 68180023007

    GET /v1/drugs/nadac/68180023007

Use it

Look up 68180-230 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-230. 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.