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United States Β· US Β· US:0074-1539_8bf84b15-6763-41cf-bfa4-bcee9ad4ef9a

Humira

SPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAbbVie Inc.
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    0074153903
    3 KIT in 1 CARTON (0074-1539-03) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .4 mL in 1 SYRINGE * 1 mL in 1 PACKET * 1 SYRINGE in 1 TRAY / .8 mL in 1 SYRINGE

Annotations

DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": null,
  "spl_meta": {
    "4977567e-3525-44ac-9ff5-f1e74b053950": {
      "match": "brand_token",
      "title": "HUMIRA (ADALIMUMAB) KIT [CORDAVIS LIMITED]",
      "spl_version": "4",
      "published_date": "2026-02-26"
    }
  },
  "productid": "0074-1539_8bf84b15-6763-41cf-bfa4-bcee9ad4ef9a",
  "productndc": "0074-1539",
  "dosage_form": "KIT",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": null,
  "proprietary_name": "Humira",
  "active_ingred_unit": null,
  "application_number": "BLA125057",
  "marketing_category": "BLA",
  "nonproprietary_name": "Adalimumab",
  "start_marketing_date": "20170421",
  "active_numerator_strength": null
}

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Humira (US) β€” Drug Database