NDC product

Estradiol

NDC 0591-0528 · Actavis Pharma, Inc.

Key facts

Product NDC 0591-0528
Proprietary name Estradiol
Labeler Actavis Pharma, Inc.
Marketing category ANDA
Application number ANDA040114
Marketing start Mar 14, 1996
Marketing end Dec 31, 2017
Listing certified through Dec 31, 2017

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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