NDC product

Levothyroxine Sodium

NDC 24236-387 · REMEDYREPACK INC.

Key facts

Product NDC 24236-387
Proprietary name Levothyroxine Sodium
Labeler REMEDYREPACK INC.
Marketing category NDA
Application number NDA021210
Marketing start Feb 18, 2013
Marketing end Feb 18, 2014
Listing certified through Feb 18, 2014

At a glance

  • 1–9 Package NDCs

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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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