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However, less than 2 weeks later, after intense public backlash and a lawsuit from compounding pharmacies, the FDA announced to the Alliance for Pharmacy Compounding that it would reevaluate their decision and not take action against pharmacies who continue selling the compounded version
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10.1212/wnl.57.8.1422 Neurology 58 OhgamiR
Conversely, keeping them restricted forces pharmacies to enforce strict quality audits and avoid these active pharmaceutical ingredients (APIs) entirely
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