NDC product

Ludiomil

NDC 0083-0135 · Novartis Pharmaceuticals Corporation

Key facts

Product NDC 0083-0135
Proprietary name Ludiomil
Labeler Novartis Pharmaceuticals Corporation
Marketing category NDA
Application number NDA017543
Marketing start Dec 1, 1980
Marketing end Oct 30, 2008
Listing certified through Oct 30, 2008

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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