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Zdrowie i gospodarka · 17/02/2023

FDA Clears Dihydroergotamine Mesylate 45 Injection for Continued Sale

The US Food and Drug Administration (FDA) has ruled that D.H.E. 45 injection, a medication used to treat migraines, will not be removed from the market due to safety or effectiveness concerns, allowing it to remain available for future abbreviated new drug applications (ANDAs).

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