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Lacosamide

NDC 60687-676, Lacosamide, tablet, film coated, from American Health Packaging.

Product NDC
60687-676
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214695
DEA schedule
CV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60687-676 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACOSAMIDE50 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
60687-676-576068706765760 BLISTER PACK in 1 CARTON (60687-676-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-676-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/19060029-c158-4a37-9261-cfe3b2b5b1e3

  • NADAC price for package 60687067657

    GET /v1/drugs/nadac/60687067657

Use it

Look up 60687-676 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-676 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-676. 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.