humira

Generic: adalimumab

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name humira
Generic Name adalimumab
Labeler a-s medication solutions
Dosage Form KIT
Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4487
Product ID 50090-4487_9083dedd-bfe5-47f1-b940-72101f343d9d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA125057
Listing Expiration 2026-12-31
Marketing Start 2006-06-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904487
Hyphenated Format 50090-4487

Supplemental Identifiers

RxCUI
797544 1655726 1655728

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name humira (source: ndc)
Generic Name adalimumab (source: ndc)
Application Number BLA125057 (source: ndc)

Resolved Composition

Strengths
  • 80 mg/0.8 ml
  • 40 mg/0.8 ml
  • 40 mg/0.4 ml
  • 20 mg/0.4 ml
  • 20 mg/0.2 ml
  • 10 mg/0.2 ml
  • 10 mg/0.1 ml
  • 1 ml
source: label
Packaging
  • 2 KIT in 1 CARTON (50090-4487-0) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .8 mL in 1 SYRINGE * 1 mL in 1 PACKET
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "9083dedd-bfe5-47f1-b940-72101f343d9d", "openfda": {"rxcui": ["797544", "1655726", "1655728"], "spl_set_id": ["a06a9aec-fd5b-4c3e-a81f-eb46bb384100"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 KIT in 1 CARTON (50090-4487-0)  / 1 KIT in 1 KIT *  1 SYRINGE in 1 TRAY / .8 mL in 1 SYRINGE *  1 mL in 1 PACKET", "package_ndc": "50090-4487-0", "marketing_start_date": "20190829"}], "brand_name": "HUMIRA", "product_id": "50090-4487_9083dedd-bfe5-47f1-b940-72101f343d9d", "dosage_form": "KIT", "product_ndc": "50090-4487", "generic_name": "Adalimumab", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HUMIRA", "application_number": "BLA125057", "marketing_category": "BLA", "marketing_start_date": "20060623", "listing_expiration_date": "20261231"}