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FDAs April 1 example appears directed at that post-shortage playbook and signals that the agency may view many semaglutide-plus-additive products as remaining essentially copies, absent robust, individualized clinical justification
doi:10.1371/journal.pone.0037290
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(PubMed) Brass EP, Koster D, Hiatt WR, Amato A
Kimura, S
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