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Lacosamide

NDC 69367-351, Lacosamide, tablet, film coated, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-351
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205237
DEA schedule
CV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACOSAMIDE200 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
69367-351-606936703516060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-351-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ecb8b33e-7cbd-4f5e-9fe9-e72dff9bcb86

  • NADAC price for package 69367035160

    GET /v1/drugs/nadac/69367035160

Use it

Look up 69367-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-351. 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.