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Memantine Hydrochloride

NDC 61442-192, Memantine Hydrochloride, tablet, film coated, from Carlsbad Technology, Inc..

Product NDC
61442-192
Status
Listed
Labeler
Carlsbad Technology, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212947
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/61442-192 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEMANTINE HYDROCHLORIDE5 mg/1

Pharmacologic classes

N-methyl-D-aspartate Receptor Antagonist [EPC]; NMDA Receptor Antagonists [MoA]

Package NDCNDC-11Package
61442-192-0561442019205500 TABLET, FILM COATED in 1 BOTTLE (61442-192-05)
61442-192-606144201926060 TABLET, FILM COATED in 1 BOTTLE (61442-192-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/30b4d5c4-0a31-c385-e063-6394a90adbce

  • NADAC price for package 61442019205

    GET /v1/drugs/nadac/61442019205

Use it

Look up 61442-192 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/61442-192 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 61442-192. 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.