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Memantine Hydrochloride

NDC 65862-652, Memantine Hydrochloride, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-652
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203175
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-652 \
  -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
65862-652-03658620652033 BLISTER PACK in 1 CARTON (65862-652-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-652-10)
65862-652-606586206526060 TABLET, FILM COATED in 1 BOTTLE (65862-652-60)
65862-652-786586206527810 BLISTER PACK in 1 CARTON (65862-652-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-652-10)
65862-652-99658620652991000 TABLET, FILM COATED in 1 BOTTLE (65862-652-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ceb733fa-4526-4b76-ab6a-bd4c5638afff

Use it

Look up 65862-652 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-652 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-652. 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.