ZEPOSIA 7-Day Starter Pack
NDC 59572-810, ozanimod hydrochloride, kit, from Celgene Corporation.
- Product NDC
- 59572-810
- Status
- Listed
- Labeler
- Celgene Corporation
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA209899
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59572-810 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59572-810-07 | 59572081007 | 1 KIT in 1 BLISTER PACK (59572-810-07) * 1 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACK |
| 59572-810-97 | 59572081097 | 1 KIT in 1 BLISTER PACK (59572-810-97) * 1 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/93ce2fab-edfb-4804-8074-963071de51e4
Use it
Look up 59572-810 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59572-810 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59572-810. 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.