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Memantine hydrochloride

NDC 33342-221, Memantine hydrochloride, capsule, extended release, from Macleods Pharmaceuticals Limited.

Product NDC
33342-221
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206310
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-221 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEMANTINE HYDROCHLORIDE21 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
33342-221-073334202210730 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-221-07)
33342-221-123334202211210 BLISTER PACK in 1 CARTON (33342-221-12) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/62e32b0b-1eb2-424d-bfd2-d27ef27d35f3

Use it

Look up 33342-221 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-221 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-221. 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.