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Memantine Hydrochloride

NDC 47335-321, Memantine Hydrochloride, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-321
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090058
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-321 \
  -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
47335-321-0847335032108100 TABLET, FILM COATED in 1 BOTTLE (47335-321-08)
47335-321-18473350321181000 TABLET, FILM COATED in 1 BOTTLE (47335-321-18)
47335-321-864733503218660 TABLET, FILM COATED in 1 BOTTLE (47335-321-86)
47335-321-8847335032188100 TABLET, FILM COATED in 1 BOTTLE (47335-321-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d1963395-3cf7-4433-bf2c-06295bb1c5b0

  • NADAC price for package 47335032186

    GET /v1/drugs/nadac/47335032186

Use it

Look up 47335-321 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-321 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-321. 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.