NDC product

ZOLEDRONIC ACID

NDC 0409-4215 · Hospira, Inc.

Key facts

Product NDC 0409-4215
Proprietary name ZOLEDRONIC ACID
Labeler Hospira, Inc.
Marketing category ANDA
Application number ANDA090621
Marketing start Oct 19, 2017
Marketing end Oct 1, 2023
Listing certified through Oct 1, 2023

At a glance

  • 1–9 Package NDCs

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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:

Browse all National Drug Codes (NDC)