BRIEF-Mannkind Announces U.S. FDA Accepts For Review Its Supplemental New Drug Application (SNDA) Of Furoscix Readyflow™ Autoinjector

Reuters

2025/12/01

BRIEF-Mannkind Announces U.S. FDA Accepts For Review Its Supplemental New Drug Application <a href="https://laohu8.com/S/SNDA">$(SNDA)$</a> 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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