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Business · 31/01/2018Updated: 10/17/2026 · 1 min read

FDA Determines Regulatory Review Period for CRESEMBA Patent Extension

Summary

The US Food and Drug Administration has officially approved the regulatory review period for the patent extension of CRESEMBA, a drug approved under the new drug application 207501, following a submission to the US Patent and Trademark Office.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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