Brief: Mannkind Announces U.S. FDA Accepts For Review Its Supplemental New Drug Application (SNDA) Of Furoscix Readyflow™ Autoinjector
Dec 1 (Reuters) - MannKind Corp MNKD.O: MANNKIND ANNOUNCES U.S. FDA ACCEPTS FOR REVIEW ITS SUPPLEMENTAL NEW DRUG APPLICATION (SNDA) OF FUROSCIX READYFLOW™ AUTOINJECTOR FOR THE TREATMENT OF EDEMA IN ADULTS WITH CHRONIC HEART FAILURE OR CHRONIC KIDNEY DISEASE MANNKIND CORP - PDUFA TARGET ACTION DATE SET FOR JULY 26, 2026 Source text: ID:nGNX9rqQK6 Further company coverage: MNKD.O ((Reuters.Briefs@thomsonreuters.com;))
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