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Monthly Prescribing Reference
9h
FDA Drug Approval Decisions Expected in November 2024
The Prescription Drug User Fee Act (PDUFA) date refers to the deadline set by the US Food and Drug Administration (FDA) for reviewing a New Drug ...
Monthly Prescribing Reference
13h
Navenibart Gets Orphan Drug Status for Hereditary Angioedema
The Food and Drug Administration (FDA) has granted Orphan Drug designation to navenibart for the treatment of hereditary angioedema (HAE).
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