The FDA has launched a free mobile app version of its Drugs@FDA online database that offers consumers information on agency-approved drugs. The new app, called Drugs@FDA Express, is free and currently ...
The U.S. Food and Drug Administration (FDA) has granted traditional approval to Jaypirca (pirobrutinib) for the treatment of ...
The U.S. Food and Drug Administration (FDA) has approved Breyanzi (lisocabtagene maraleucel) for the treatment of adults with relapsed or refractory marginal zone lymphoma who have received at least ...
In October 2025, the FDA released a revised guidance titled, “Expanded Access to Investigational Drugs for Treatment Use—Questions and Answers.” ...
If your summer skincare looks more like dessert than SPF, the Food and Drug Administration (FDA) has a message: Put down the whipped cream canister—especially if it’s sunscreen. On Monday, the agency ...
Compounded tirzepatide contains the same active ingredient as Mounjaro, but its dosage and some ingredients may differ from Mounjaro. The Food and Drug Administration (FDA) does not regulate the ...
(NewsNation) — The Food and Drug Administration launched a crackdown on misleading pharmaceutical advertising Tuesday, sending thousands of warning letters and approximately 100 cease-and-desist ...
The U.S. Food and Drug Administration has issued warning letters to five popular sunscreen brands over their mousse products. The federal regulator is also urging consumers not to use the foam-style ...
As COVID-19 swept across the globe in early 2020, the Food and Drug Administration (FDA) pulled most of its safety inspectors from the field, creating a massive backlog of uninspected pharmaceutical ...
The Food and Drug Omnibus Reform Act of 2022 (“FDORA” or the “Act”), signed into law on December 29, 2022,[1] required, in part, drug and device manufacturers to submit Diversity Action Plans to the U ...
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