NDC product

Thiopental Sodium

NDC 0409-6431 · Hospira, Inc.

Key facts

Product NDC 0409-6431
Proprietary name Thiopental Sodium
Labeler Hospira, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start May 25, 2010
Marketing end Jan 21, 2011
Listing certified through Jan 21, 2011

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)