Dietary supplement firms already acting on a 2014 proposed rule by preparing to declare added sugars on product labels will have to find more room to add the daily percentage of total energy intake contained in a product’s added sugars under FDA’s additions to the proposal.
Additional Sugar Label Requirements Taste Sour To Supplement Industry
FDA proposes revisions to a 2014 proposed rule due to the 2015 Dietary Guideline Advisory Committee’s report. In a supplemental proposed rule, FDA will establish a daily reference value of 10% of total energy intake from added sugars and require label declarations of the percent daily value for added sugars.
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Organizational turmoil has not yet affected reviews of novel agent applications, with Q1 2025 approvals coming in low, but the first quarter share of the entire year is variable.
Most, if not all, adcomm support staff in the drug and biologic centers who handled meeting-specific tasks have been laid off, although sponsors still are preparing for the public reviews. Meanwhile, some cut FDA employees are being called back to work for "continuity of operations activities."
Product reviews for drugs, biologics, devices, tobacco and foods could be consolidated into one office at the FDA, as part of a restructuring plan circulating that was obtained by Pink Sheet.
Pink Sheet reporter and editors discuss how the massive layoffs will reshape the FDA and its impact on the drug and biologics industries.
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Trump announced a 26% reciprocal tariff on India, but a country-agnostic exemption of pharmaceuticals implies that the interests of Indian firms are protected for now. What is Indian pharma’s business exposure and what is domestic industry saying?