NDC product

Elestrin

NDC 18860-490 · Azur Pharma Inc.

Key facts

Product NDC 18860-490
Proprietary name Elestrin
Labeler Azur Pharma Inc.
Marketing category NDA
Application number NDA021813
Marketing start Jun 1, 2007
Marketing end Sep 24, 2010
Listing certified through Sep 24, 2010

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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