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FDA Seeks Input On Inactive Ingredients Database

US Agency Plans To Prioritize Maximum Daily Exposure Information

 
• By Dave Wallace

Industry input is being sought by the FDA on its inactive ingredient database, as the US agency considers how to prioritize the addition of maximum daily exposure limits as well as mulling the removal of specific dosage form information.

Grunge red inactive word with star icon round rubber seal stamp on white background
The FDA is seeking feedback on changes to its inactive ingredient database • Source: Thanee Hengpattanapong / Alamy Stock Vector

Input is being solicited by the US Food and Drug Administration on how best to prioritize the addition of maximum daily exposure information to its inactive ingredient database, as well as potentially modifying the IID structure to eliminate dosage form information.

Interested parties have until 21 June to submit comments to the FDA either electronically or in writing, with full details available at the Federal Register.

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