NDC product

Ximino

NDC 10631-331 · Sun Pharmaceutical Industries, Inc

Key facts

Product NDC 10631-331
Proprietary name Ximino
Labeler Sun Pharmaceutical Industries, Inc
Marketing category NDA
Application number NDA201922
Marketing start Oct 25, 2017
Marketing end Aug 31, 2022
Listing certified through Aug 31, 2022

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:

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