NDC product

Angiomax

NDC 0781-3447 · Sandoz Inc

Key facts

Product NDC 0781-3447
Proprietary name Angiomax
Labeler Sandoz Inc
Marketing category NDA
Application number NDA020873
Marketing start Aug 1, 2019
Marketing end Jun 30, 2023
Listing certified through Jun 30, 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)