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memantine hydrochloride

NDC 31722-808, memantine hydrochloride, tablet, from Camber Pharmaceuticals, Inc..

Product NDC
31722-808
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204389
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-808 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEMANTINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

N-methyl-D-aspartate Receptor Antagonist [EPC]; NMDA Receptor Antagonists [MoA]

Package NDCNDC-11Package
31722-808-0231722080802200 TABLET in 1 BOTTLE (31722-808-02)
31722-808-323172208083210 BLISTER PACK in 1 CARTON (31722-808-32) / 10 TABLET in 1 BLISTER PACK
31722-808-603172208086060 TABLET in 1 BOTTLE (31722-808-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/910827aa-5320-446c-8f66-3f17c0ee36d9

  • NADAC price for package 31722080860

    GET /v1/drugs/nadac/31722080860

Use it

Look up 31722-808 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-808 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-808. 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.