XELJANZ XR
NDC 63539-502, tofacitinib, tablet, extended release, from U.S. Pharmaceuticals.
- Product NDC
- 63539-502
- Status
- Listed
- Labeler
- U.S. Pharmaceuticals
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA208246
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63539-502 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TOFACITINIB CITRATE22 mg/1
Pharmacologic classes
Janus Kinase Inhibitor [EPC]; Janus Kinase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63539-502-30 | 63539050230 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63539-502-30) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/68e3d6b2-7838-4d2d-a417-09d919b43e13
Use it
Look up 63539-502 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63539-502 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63539-502. 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.