NDC product

SUPRAX

NDC 27437-203 · LUPIN PHARMA

Key facts

Product NDC 27437-203
Proprietary name SUPRAX
Labeler LUPIN PHARMA
Marketing category ANDA
Application number ANDA065380
Marketing start Oct 11, 2012
Marketing end Jun 21, 2013
Listing certified through Jun 21, 2013

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)