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ZEPOSIA Starter Kit

NDC 59572-890, ozanimod hydrochloride, kit, from Celgene Corporation.

Product NDC
59572-890
Status
Listed
Labeler
Celgene Corporation
Dosage form
KIT
Route
—
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA209899
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59572-890 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
59572-890-28595720890281 KIT in 1 CARTON (59572-890-28) * 1 CAPSULE in 1 BLISTER PACK * 21 CAPSULE in 1 BOTTLE, PLASTIC * 1 CAPSULE in 1 BLISTER PACK
59572-890-98595720890981 KIT in 1 CARTON (59572-890-98) * 1 CAPSULE in 1 BLISTER PACK * 21 CAPSULE in 1 BOTTLE, PLASTIC * 1 CAPSULE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/93ce2fab-edfb-4804-8074-963071de51e4

Use it

Look up 59572-890 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59572-890 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59572-890. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.