NDC product

AlleRx Dose Pack

NDC 10122-650 · Cornerstone Therapeutics Inc.

Key facts

Product NDC 10122-650
Proprietary name AlleRx
Labeler Cornerstone Therapeutics Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start Feb 1, 2008
Marketing end Oct 31, 2012
Listing certified through Oct 31, 2012

At a glance

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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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