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Memantine hydrochloride

NDC 70771-1321, Memantine hydrochloride, capsule, extended release, from Zydus Lifesciences Limited.

Product NDC
70771-1321
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203293
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1321 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEMANTINE HYDROCHLORIDE7 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70771-1321-37077113210330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1321-3)
70771-1321-47077113210410 BLISTER PACK in 1 CARTON (70771-1321-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1321-2)
70771-1321-97077113210990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1321-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ec825bef-2313-45c2-8858-b43197680155

Use it

Look up 70771-1321 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1321 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1321. 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.