NDC 0074-3799

Humira

Adalimumab

Humira is a Kit in the Human Prescription Drug category. It is labeled and distributed by Abbvie Inc.. The primary component is .

• Product ID: 0074-3799_05cc7e8b-7ac7-6196-0260-f15f8aad95ba
• NDC: 0074-3799
• Product Type: Human Prescription Drug
• Proprietary Name: Humira
• Generic Name: Adalimumab
• Dosage Form: Kit
• Marketing Start Date: 2002-12-31
• Marketing Category: BLA / BLA
• Application Number: BLA125057
• Labeler Name: AbbVie Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0074-3799-02

2 KIT in 1 CARTON (0074-3799-02) > 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY > .8 mL in 1 SYRINGE * 1 mL in 1 PACKET

• Marketing Start Date: 2002-12-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0074-3799-71 [00074379971]

Humira KIT

• Marketing Category: BLA
• Application Number: BLA125057
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2002-12-31
• Marketing End Date: 2019-11-30

NDC 0074-3799-01 [00074379901]

Humira KIT

• Marketing Category: BLA
• Application Number: BLA125057
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2002-12-31
• Marketing End Date: 2010-08-10

NDC 0074-3799-06 [00074379906]

Humira KIT

• Marketing Category: BLA
• Application Number: BLA125057
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2002-12-31

NDC 0074-3799-02 [00074379902]

Humira KIT

• Marketing Category: BLA
• Application Number: BLA125057
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2002-12-31

NDC 0074-3799-03 [00074379903]

Humira KIT

• Marketing Category: BLA
• Application Number: BLA125057
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2002-12-31

Drug Details

OpenFDA Data

• SPL SET ID: 608d4f0d-b19f-46d3-749a-7159aa5f933d
• Manufacturer:
  • AbbVie Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 1921238
  • 727705
  • 727703
  • 1655726
  • 797544
  • 763565
  • 763564
  • 1921010
  • 825169
  • 1655728
  • 1921009
  • 1656703
  • 352334
  • 1551888
  • 1872980
  • 1921468
  • 1551887
  • 1921467
  • 1594357
  • 1594352
  • 1594358
  • 1921244
  • 1921245
  • 351290
  • 1921240
  • 1801277
  • 825170
  • 1872986
  • 1872984
  • 1872985
  • 1872983
  • 1801278
  • 1873086
  • 1873087
  • 1921017
  • 1921016
  • 1726846
  • 1726844
  • 1855527
  • 1855526
  • 1872979
  • 1855524
  • 1855523

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