humira
Generic: adalimumab
Labeler: abbvie inc.Drug Facts
Product Profile
Brand Name
humira
Generic Name
adalimumab
Labeler
abbvie inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
0074-3799
Product ID
0074-3799_8bf84b15-6763-41cf-bfa4-bcee9ad4ef9a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
BLA
Application Number
BLA125057
Listing Expiration
2027-12-31
Marketing Start
2002-12-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00743799
Hyphenated Format
0074-3799
Supplemental Identifiers
RxCUI
Packaging Origin
Original Packager
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/0.2 ml
- 10 mg/0.1 ml
- 1 ml
Packaging
- 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
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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