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memantine hydrochloride

NDC 0591-3900, memantine hydrochloride, kit, from Actavis Pharma, Inc..

Product NDC
0591-3900
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
KIT
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/0591-3900 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
0591-3900-87005913900871 BLISTER PACK in 1 CARTON (0591-3900-87) / 1 KIT in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

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

Use it

Look up 0591-3900 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3900 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0591-3900. 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.