The US Food and Drug Administration has unleashed a potentially prolific source of hydroxychloroquine sulfate tablets, under investigation for efficacy against the COVID-19 coronavirus, by adding the approved malaria, lupus and rheumatoid arthritis treatment on 25 March to the list of drugs that outsourcing facilities regulated under Section 503B of the Food, Drug and Cosmetic Act are allowed to compound from bulk ingredients.
In the meantime, the Alliance for Pharmacy Compounders urged the FDA to place more prescription and over-the-counter drugs on the list of drugs that can be
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