PONVORY
NDC 50458-720, Ponesimod, tablet, film coated, from Janssen Pharmaceuticals, Inc.
- Product NDC
- 50458-720
- Status
- Listed
- Labeler
- Janssen Pharmaceuticals, Inc
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA213498
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50458-720 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PONESIMOD20 mg/1
Pharmacologic classes
Sphingosine 1-Phosphate Receptor Modulators [MoA]; Sphingosine 1-phosphate Receptor Modulator [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50458-720-30 | 50458072030 | 1 BOTTLE in 1 CARTON (50458-720-30) / 30 TABLET, FILM COATED in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5be69660-738c-4db7-b0d4-517aa873dc41
Use it
Look up 50458-720 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50458-720 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50458-720. 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.