NDC 59572-502

Pomalyst

Pomalidomide

Pomalyst is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Celgene Corporation. The primary component is Pomalidomide.

• Product ID: 59572-502_0e50dfc9-35ac-4b11-89f1-5c3653717c3d
• NDC: 59572-502
• Product Type: Human Prescription Drug
• Proprietary Name: Pomalyst
• Generic Name: Pomalidomide
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 2013-02-18
• Marketing Category: NDA / NDA
• Application Number: NDA204026
• Labeler Name: Celgene Corporation
• Substance Name: POMALIDOMIDE
• Active Ingredient Strength: 2 mg/1
• Pharm Classes: Thalidomide Analog [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 59572-502-00

100 CAPSULE in 1 BOTTLE (59572-502-00)

• Marketing Start Date: 2013-02-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59572-502-00 [59572050200]

Pomalyst CAPSULE

• Marketing Category: NDA
• Application Number: NDA204026
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2013-02-18

NDC 59572-502-21 [59572050221]

Pomalyst CAPSULE

• Marketing Category: NDA
• Application Number: NDA204026
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2013-02-18

Drug Details

Active Ingredients

Ingredient	Strength
POMALIDOMIDE	2 mg/1

OpenFDA Data

• SPL SET ID: 2b25ef01-5c9e-11e1-b86c-0800200c9a66
• Manufacturer:
  • Celgene Corporation
• UNII:
  • D2UX06XLB5
• RxNorm Concept Unique ID - RxCUI:
  • 1369718
  • 1369734
  • 1369726
  • 1369736
  • 1369724
  • 1369730
  • 1369732
  • 1369728
• UPC Code:
  • 0359572504004

Pharmacological Class

• Thalidomide Analog [EPC]

NDC Crossover Matching brand name "Pomalyst" or generic name "Pomalidomide"

NDC	Brand Name	Generic Name
59572-501	Pomalyst	pomalidomide
59572-502	Pomalyst	pomalidomide
59572-503	Pomalyst	pomalidomide
59572-504	Pomalyst	pomalidomide