NDC product

Mannitol

NDC 0409-7715 · Hospira, Inc.

Key facts

Product NDC 0409-7715
Proprietary name Mannitol
Labeler Hospira, Inc.
Marketing category NDA
Application number NDA019603
Marketing start Sep 19, 2005
Marketing end Dec 8, 2021
Listing certified through Dec 8, 2021

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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