NDC product

CRIXIVAN

NDC 0006-0570 · Merck Sharp & Dohme LLC

Key facts

Product NDC 0006-0570
Proprietary name CRIXIVAN
Labeler Merck Sharp & Dohme LLC
Marketing category NDA
Application number NDA020685
Marketing start Mar 13, 1996
Marketing end Dec 31, 2012
Listing certified through Dec 31, 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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