NDC product

Activella

NDC 0169-5174 · Novo Nordisk

Key facts

Product NDC 0169-5174
Proprietary name Activella
Labeler Novo Nordisk
Marketing category NDA
Application number NDA020907
Marketing start Jul 22, 2003
Marketing end Oct 31, 2018
Listing certified through Oct 31, 2018

At a glance

  • 1–9 Package NDCs

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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:

Browse all National Drug Codes (NDC)