NDC 59572-810

ZEPOSIA 7-Day Starter Pack

Ozanimod Hydrochloride

ZEPOSIA 7-Day Starter Pack is a Kit in the Human Prescription Drug category. It is labeled and distributed by Celgene Corporation. The primary component is .

• Product ID: 59572-810_1059a5c1-5e0d-4320-a758-50c513ba68dd
• NDC: 59572-810
• Product Type: Human Prescription Drug
• Proprietary Name: ZEPOSIA 7-Day Starter Pack
• Generic Name: Ozanimod Hydrochloride
• Dosage Form: Kit
• Marketing Start Date: 2020-03-27
• Marketing Category: NDA / NDA
• Application Number: NDA209899
• Labeler Name: Celgene Corporation
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 59572-810-07

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

• Marketing Start Date: 2020-03-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59572-810-97 [59572081097]

ZEPOSIA 7-Day Starter Pack KIT

• Marketing Category: NDA
• Application Number: NDA209899
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-03-27

NDC 59572-810-07 [59572081007]

ZEPOSIA 7-Day Starter Pack KIT

• Marketing Category: NDA
• Application Number: NDA209899
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-03-27

Drug Details

OpenFDA Data

• SPL SET ID: 93ce2fab-edfb-4804-8074-963071de51e4
• Manufacturer:
  • Celgene Corporation
• UNII:
  • 3UPR33JAAM
• RxNorm Concept Unique ID - RxCUI:
  • 2288432
  • 2288433
  • 2288430
  • 2288431
  • 2288418
  • 2288420
  • 2288414
  • 2288406
  • 2288416
  • 2288412

NDC Crossover Matching brand name "ZEPOSIA 7-Day Starter Pack" or generic name "Ozanimod Hydrochloride"

NDC	Brand Name	Generic Name
59572-810	ZEPOSIA	ozanimod hydrochloride
59572-820	ZEPOSIA	ozanimod hydrochloride
59572-890	ZEPOSIA	ozanimod hydrochloride