Unapproved New Drugs/Misbranded/Botox
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FDA Drug Competition Action Plan
FDA’s Drug Competition Action Plan (DCAP) encourages robust and timely market competition for generic drugs and helps bring greater efficiency and transparency to the generic drug review process, without sacrificing the scientific rigor underlying our generic drug program.FDA Grand Rounds – Anti-biofilm Technologies for Enhancing the Safety of Medical Device Surfaces – 05/29/2025
Anti-biofilm Technologies for Enhancing the Safety of Medical Device Surfaces, May 29, 2025.Endothelin Receptor Antagonist REMS Information
FDA has determined that a REMS is no longer necessary to ensure ERA medicines’ benefits outweigh the risk of EFT.Libby Laboratories, Inc. – 708259 – 06/27/2025
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CGMP/Finished Pharmaceuticals/AdulteratedFood To Live Voluntarily Recalls Organic Moringa Products Because of Possible Health Risk
Brooklyn, NY – Food To Live, of Brooklyn, NY, is recalling its packaged Organic Moringa Leaf Powder (dried Moringa oleifera) and its Organic Supergreens Powder Mix distributed under the Food To Live brand that are in the following sizes:
