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Paratek Pharmaceuticals Announces FDA Orphan Drug Designation for NUZYRA (omadacycline) for the Treatment of Infections Caused by Nontuberculous Mycobacteria firstwordpharma
August 19, 2021Paratek Pharmaceuticals, Inc. today announced that the U.S. Food and Drug Administration (FDA) has granted the company orphan drug designation for NUZYRA? (omadacycline) for the treatment of infections -
Paratek Announces FDA Approval of NUZYRA? for Treatment of Community-Acquired Bacterial Pneumonia americanpharmaceuticalreview
June 04, 2021Paratek Pharmaceuticals Inc. announced that the U.S. FDA has approved the Company’s supplemental New Drug Application (sNDA) for the oral-only dosing regimen of NUZYRA? for the treatment of adults with Community-Acquired Bacterial Pneumonia (CABP). -
Paratek Gets BARDA Funding for NUZYRA Supply contractpharma
April 03, 2020To support the development and manufacturing activities of NUZYRA for the treatment of pulmonary anthrax. -
Paratek Submits pre-Emergency Use Authorization Application for NUZYRA americanpharmaceuticalreview
March 12, 2020Paratek Pharmaceuticals announced that a pre-emergency use authorization (EUA) application for NUZYRA (omadacycline) has been submitted to the U.S. Food and Drug Administration (FDA).
Pharma Sources Insight January 2025
