US FDA Seeks Ability To Include More Inactive Ingredient, Excipient Info In Brand Labeling

Additions could help streamline generic development, Center for Drug Evaluation and Research Director Patrizia Cavazzoni says.

Squeegee clears window with clouds
The FDA wants to provide a clearer picture of the inactive ingredients and excipients used in brand drugs to streamline generic development. • Source: Alamy

Generic sponsors could find more inactive ingredient and excipient information in reference product labels going forward as the US Food and Drug Administration looks for additional ways to speed drug competition to the market.

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Generics

More from Biosimilars & Generics