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memantine hydrochloride

NDC 0591-3870, memantine hydrochloride, tablet, from Actavis Pharma, Inc..

Product NDC
0591-3870
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021487
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3870 \
  -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
0591-3870-440059138704410 BLISTER PACK in 1 BOX, UNIT-DOSE (0591-3870-44) / 10 TABLET in 1 BLISTER PACK (0591-3870-45)
0591-3870-600059138706060 TABLET in 1 BOTTLE (0591-3870-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/72973b46-f307-4a9e-8fb1-ad2cbccfd736

  • NADAC price for package 00591387044

    GET /v1/drugs/nadac/00591387044

  • NADAC price for package 00591387060

    GET /v1/drugs/nadac/00591387060

Use it

Look up 0591-3870 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3870 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0591-3870. 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.