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Memantine Hydrochloride

NDC 71335-1732, Memantine Hydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-1732
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/71335-1732 \
  -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
71335-1732-17133517320130 TABLET in 1 BOTTLE (71335-1732-1)
71335-1732-27133517320260 TABLET in 1 BOTTLE (71335-1732-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9cfddd01-6e1d-4ee0-9310-3fb371724e3d

Use it

Look up 71335-1732 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1732 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-1732. 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.