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Memantine Hydrochloride

NDC 71335-2013, Memantine Hydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2013
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090961
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2013 \
  -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
71335-2013-17133520130130 TABLET in 1 BOTTLE (71335-2013-1)
71335-2013-27133520130228 TABLET in 1 BOTTLE (71335-2013-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8bd5b908-f46a-4ced-9408-45984d716149

Use it

Look up 71335-2013 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2013 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2013. 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.