LAMICTAL ODT
NDC 0173-0780, lamotrigine, kit, from GlaxoSmithKline LLC.
- Product NDC
- 0173-0780
- Status
- Listed
- Labeler
- GlaxoSmithKline LLC
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA022251
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0173-0780 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0173-0780-00 | 00173078000 | 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0173-0780-00) / 1 KIT in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/d7e3572d-56fe-4727-2bb4-013ccca22678
Use it
Look up 0173-0780 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0173-0780 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0173-0780. 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.