Mulpleta
NDC 59630-551, Lusutrombopag, tablet, film coated, from SHIONOGI INC..
- Product NDC
- 59630-551
- Status
- Listed
- Labeler
- SHIONOGI INC.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA210923
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59630-551 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LUSUTROMBOPAG3 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59630-551-07 | 59630055107 | 1 DOSE PACK in 1 CARTON (59630-551-07) / 7 TABLET, FILM COATED in 1 DOSE PACK |
| 59630-551-77 | 59630055177 | 1 DOSE PACK in 1 CARTON (59630-551-77) / 7 TABLET, FILM COATED in 1 DOSE PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f9fd0cfd-717d-4a87-99bc-de7b38807e55
Use it
Look up 59630-551 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59630-551 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59630-551. 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.