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Zdrowie i gospodarka · 13/04/2022

FDA Clears TOTECT (Dexrazoxane Hydrochloride) for Injection, 500mg, for Continued Sale

The US Food and Drug Administration (FDA) has ruled that TOTECT, a 500mg injection, was not withdrawn from the market due to safety or efficacy concerns, allowing the agency to continue approving abbreviated new drug applications (ANDAs) for the product.

Source: Federal Register — Food and Drug AdministrationOpen original release →