Lacosamide
NDC 60687-698, Lacosamide, tablet, film coated, from American Health Packaging.
- Product NDC
- 60687-698
- 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
curl https://api.healthcare.dev/v1/drugs/ndc/60687-698 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 60687-698-57 | 60687069857 | 60 BLISTER PACK in 1 CARTON (60687-698-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-698-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/19060029-c158-4a37-9261-cfe3b2b5b1e3NADAC price for package 60687069857
GET /v1/drugs/nadac/60687069857
Use it
Look up 60687-698 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-698 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-698. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.