Trikafta
NDC 51167-331, Elexacaftor, Tezacaftor, and Ivacaftor, kit, from Vertex Pharmaceuticals Incorporated.
- Product NDC
- 51167-331
- Status
- Listed
- Labeler
- Vertex Pharmaceuticals Incorporated
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA212273
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51167-331 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51167-331-01 | 51167033101 | 4 BLISTER PACK in 1 CARTON (51167-331-01) / 1 KIT in 1 BLISTER PACK * 14 TABLET, FILM COATED in 1 BLISTER PACK (51167-431-14) * 7 TABLET, FILM COATED in 1 BLISTER PACK (51167-531-07) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f354423a-85c2-41c3-a9db-0f3aee135d8d
Use it
Look up 51167-331 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51167-331 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51167-331. 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.