The FDA Often Doesn’t Test Generic Drugs for Quality Concerns, So ProPublica Did

Billions of prescriptions for generic drugs are filled in the U.S. annually. The FDA tests only a few dozen of them every ...
Stocktwits on MSN

MannKind stock slips despite FDA clearing pediatric use of heart failure drug — what’s spooking investors?

The FDA expanded Furoscix use to certain pediatric patients. ・MannKind received five new U.S. patents supporting its ...
Lehigh Valley Live

Check your Christmas stockings now: FDA issues urgent recall on chocolate that has already caused an allergic reaction

Approximately 112 units of Fran’s Pure Bar Almondmilk Chocolate made by Fran’s Chocolates, Ltd. of Seattle, Washington, are ...
Flow Space on MSN

5 FDA & other guideline changes midlife women should know about that happened in 2025

2025 was a busy year for the U.S Food and Drug Administration (FDA). The federal agency granted approval to several ...

Enveda Advances Third Asset to the Clinic With US FDA IND Clearance and Phase 1 Initiation of ENV-6946, a First-in-Class Oral "Multi-Biologic in a Pill" for Inflammatory Bowel ...

Enveda, a multi-asset clinical-stage biotech company pioneering the discovery and development of a new generation of small-molecule drugs derived from life’s chemistry, today announced that the US ...
Medscape

FDA Approves Novel Fibrinogen Concentrate for CFD

The fibrinogen concentrate is approved for children and adults with acute bleeding related to certain types of congenital ...

FDA Officially Confirms Kava is a Food Under Federal Law

After Reviewing Historical Use and Modern Safety Evidence, Officially Confirms Kava is a Food Under Federal Law ...