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Levetiracetam ER

NDC 69367-332, Levetiracetam, tablet, film coated, extended release, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-332
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205130
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-332 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVETIRACETAM500 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
69367-332-606936703326060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69367-332-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c508a392-0603-477d-8a45-3ec550371111

  • NADAC price for package 69367033260

    GET /v1/drugs/nadac/69367033260

Use it

Look up 69367-332 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-332 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-332. 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.