NDC product

Oxybutynin Chloride

NDC 10135-610 · Marlex Pharmaceuticals Inc

Key facts

Product NDC 10135-610
Proprietary name Oxybutynin Chloride
Labeler Marlex Pharmaceuticals Inc
Marketing category ANDA
Application number ANDA204010
Marketing start Feb 1, 2016
Listing certified through Dec 31, 2020

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)