NDC 50090-3530

Humira

Adalimumab

Humira is a Kit in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is .

• Product ID: 50090-3530_414988b4-9b35-45c5-a0e7-e6173339e8d3
• NDC: 50090-3530
• Product Type: Human Prescription Drug
• Proprietary Name: Humira
• Generic Name: Adalimumab
• Dosage Form: Kit
• Marketing Start Date: 2006-06-23
• Marketing Category: BLA / BLA
• Application Number: BLA125057
• Labeler Name: A-S Medication Solutions
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 50090-3530-0

1 KIT in 1 KIT (50090-3530-0) * 1 mL in 1 PACKET * 1 SYRINGE in 1 TRAY > .8 mL in 1 SYRINGE

• Marketing Start Date: 2018-08-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50090-3530-0 [50090353000]

Humira KIT

• Marketing Category: BLA
• Application Number: BLA125057
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-08-01
• Marketing End Date: 2019-12-31

Drug Details

OpenFDA Data

• SPL SET ID: 26a51df4-8548-47e0-a824-d35f6b8c3cbc
• Manufacturer:
  • A-S Medication Solutions
• RxNorm Concept Unique ID - RxCUI:
  • 727705
  • 727703
  • 797544
  • 763565
  • 763564

NDC Crossover Matching brand name "Humira" or generic name "Adalimumab"

NDC	Brand Name	Generic Name
0074-0067	Humira	Adalimumab
0074-0124	Humira	Adalimumab
0074-0243	Humira	Adalimumab
0074-0554	Humira	Adalimumab
0074-0616	Humira	Adalimumab
0074-0817	Humira	Humira
0074-2540	Humira	Humira
0074-1539	Humira	Humira
0074-4339	Humira	Humira
0074-3799	Humira	Humira
0074-9374	Humira	Humira
0074-6347	Humira	Humira
50090-3530	Humira	Humira
50090-4487	Humira	Humira