NDC product

Humira

NDC 0074-3797 · AbbVie Inc.

Key facts

Product NDC 0074-3797
Proprietary name Humira
Labeler AbbVie Inc.
Marketing category BLA
Application number BLA125057
Marketing start Dec 30, 2002
Marketing end Feb 4, 2026
Listing certified through Feb 4, 2026

At a glance

  • 1–9 Package NDCs

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About National Drug Codes (NDC)

The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.

Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date:

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