USAntibiotics on Tuesday won approval for its American-made version of extended-release amoxicillin, about two months faster than normal.
It is the first product to win approval as part of FDA Commissioner Marty Makary’s
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An FDA staff analysis of the safety of pediatric Covid-19 shots has been finalized and sent to the agency’s vaccine and biologics head Vinay Prasad.
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As part of a batch of recommendations issued Friday, the European Medicines Agency’s human medicines committee (CHMP) recommended rejecting Anavex’s Alzheimer’s disease drug, issuing a
USAntibiotics on Tuesday won approval for its American-made version of extended-release amoxicillin, about two months faster than normal.
It is the first product to win approval as part of FDA Commissioner Marty Makary’s