zeposia 7-day starter pack

Generic: ozanimod hydrochloride

Labeler: celgene corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zeposia 7-day starter pack
Generic Name ozanimod hydrochloride
Labeler celgene corporation
Dosage Form KIT
Manufacturer
Celgene Corporation

Identifiers & Regulatory

Product NDC 59572-810
Product ID 59572-810_47f2242f-a571-48a8-985a-8fa4f79ec12f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA209899
Listing Expiration 2026-12-31
Marketing Start 2020-03-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59572810
Hyphenated Format 59572-810

Supplemental Identifiers

RxCUI
2288406 2288412 2288414 2288416 2288418 2288420 2288430 2288431 2288432 2288433 2642213 2642214
UNII
3UPR33JAAM

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name zeposia 7-day starter pack (source: ndc)
Generic Name ozanimod hydrochloride (source: ndc)
Application Number NDA209899 (source: ndc)
Routes
oral
source: label

Resolved Composition

Strengths
  • 0.23 mg
  • 0.46 mg
  • 0.92 mg
source: label
Packaging
  • 1 KIT in 1 BLISTER PACK (59572-810-07) * 1 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACK
  • 1 KIT in 1 BLISTER PACK (59572-810-97) * 1 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (2)

59572-810-07 1 KIT in 1 BLISTER PACK (59572-810-07) * 1 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACK 59572-810-97 1 KIT in 1 BLISTER PACK (59572-810-97) * 1 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

ZEPOSIA 7-Day Starter Pack, ZEPOSIA, ZEPOSIA Starter Kit ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "47f2242f-a571-48a8-985a-8fa4f79ec12f", "openfda": {"unii": ["3UPR33JAAM"], "rxcui": ["2288406", "2288412", "2288414", "2288416", "2288418", "2288420", "2288430", "2288431", "2288432", "2288433", "2642213", "2642214"], "spl_set_id": ["93ce2fab-edfb-4804-8074-963071de51e4"], "manufacturer_name": ["Celgene Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 BLISTER PACK (59572-810-07)  *  1 CAPSULE in 1 BLISTER PACK *  1 CAPSULE in 1 BLISTER PACK", "package_ndc": "59572-810-07", "marketing_start_date": "20200327"}, {"sample": false, "description": "1 KIT in 1 BLISTER PACK (59572-810-97)  *  1 CAPSULE in 1 BLISTER PACK *  1 CAPSULE in 1 BLISTER PACK", "package_ndc": "59572-810-97", "marketing_start_date": "20200327"}], "brand_name": "ZEPOSIA 7-Day Starter Pack", "product_id": "59572-810_47f2242f-a571-48a8-985a-8fa4f79ec12f", "dosage_form": "KIT", "product_ndc": "59572-810", "generic_name": "ozanimod hydrochloride", "labeler_name": "Celgene Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZEPOSIA", "brand_name_suffix": "7-Day Starter Pack", "application_number": "NDA209899", "marketing_category": "NDA", "marketing_start_date": "20200327", "listing_expiration_date": "20261231"}