NDC product

ANZEMET

NDC 30698-220 · Validus Pharmaceuticals LLC

Key facts

Product NDC 30698-220
Proprietary name ANZEMET
Labeler Validus Pharmaceuticals LLC
Marketing category NDA
Application number NDA020623
Marketing start Sep 11, 1997
Listing certified through Dec 31, 2024

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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