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 ID0074-3799_05cc7e8b-7ac7-6196-0260-f15f8aad95ba
NDC0074-3799
Product TypeHuman Prescription Drug
Proprietary NameHumira
Generic NameAdalimumab
Dosage FormKit
Marketing Start Date2002-12-31
Marketing CategoryBLA / BLA
Application NumberBLA125057
Labeler NameAbbVie Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2021-12-31

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 Date2002-12-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0074-3799-71 [00074379971]

Humira KIT
Marketing CategoryBLA
Application NumberBLA125057
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-12-31
Marketing End Date2019-11-30

NDC 0074-3799-01 [00074379901]

Humira KIT
Marketing CategoryBLA
Application NumberBLA125057
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-12-31
Marketing End Date2010-08-10

NDC 0074-3799-06 [00074379906]

Humira KIT
Marketing CategoryBLA
Application NumberBLA125057
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-12-31

NDC 0074-3799-02 [00074379902]

Humira KIT
Marketing CategoryBLA
Application NumberBLA125057
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-12-31

NDC 0074-3799-03 [00074379903]

Humira KIT
Marketing CategoryBLA
Application NumberBLA125057
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-12-31

Drug Details

OpenFDA Data

SPL SET ID:608d4f0d-b19f-46d3-749a-7159aa5f933d
Manufacturer
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"

    NDCBrand NameGeneric Name
    0074-0067HumiraAdalimumab
    0074-0124HumiraAdalimumab
    0074-0243HumiraAdalimumab
    0074-0554HumiraAdalimumab
    0074-0616HumiraAdalimumab
    0074-0817HumiraHumira
    0074-2540HumiraHumira
    0074-1539HumiraHumira
    0074-4339HumiraHumira
    0074-3799HumiraHumira
    0074-9374HumiraHumira
    0074-6347HumiraHumira
    50090-3530HumiraHumira
    50090-4487HumiraHumira

    Trademark Results [Humira]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    HUMIRA
    HUMIRA
    78082476 2725934 Live/Registered
    ABBVIE BIOTECHNOLOGY LTD.
    2001-09-04
    HUMIRA
    HUMIRA
    77831297 3784305 Live/Registered
    ABBVIE BIOTECHNOLOGY LTD.
    2009-09-21

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