NDC product

Novolin 70/30

NDC 0169-3477 · Novo Nordisk

Key facts

Product NDC 0169-3477
Proprietary name Novolin
Labeler Novo Nordisk
Marketing category NDA
Application number NDA019991
Marketing start Jun 25, 1991
Marketing end Jul 17, 2012
Listing certified through Jul 17, 2012

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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