Strides Pharma shares hit 52-week high on USFDA nod to heart disease drug
Shares of the pharma firm zoomed 8.02% to Rs 538.65 in early deals against the previous close of Rs 498.65 on BSE.
FDA advisory panel rejects drug-device combination to treat Type 2 diabetes
The vote essentially upheld the Food and Drug Administration’s earlier rulings, with some members calling for new clinical ...
Stockhead on MSN2h
FDA approves commercial brand name for Dimerix’s kidney disease drug
The US Food and Drug Administration (FDA) has given Dimerix conditional approval for the brand name QYTOVRA for ... Read More ...
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Food and Drug Administration approves COVID boosters for upcoming season
An advisory panel at the CDC is scheduled to vote on recommendations Tuesday, the final step in the process before people can ...
Palm Beach Post24d
U.S. Food and Drug Administration is warning people to stop using two eye drop products
The U.S. Food and Drug Administration is warning people to stop using two more eye drop products after the agency found bacterial contamination in some of them. According to a notice posted on ...
WWNO13d
The Food and Drug Administration is poised to approve new COVID boosters
The latest shots could bolster immunity as a new COVID-19 wave rises, and the season for peak respiratory illnesses approaches.
CBS News17d
FDA warns consumers not to eat certain oysters from Connecticut over potential sewage contamination
00:30 Oysters harvested in Connecticut and distributed to restaurants and stores across five states could be contaminated by sewage, the Food and Drug Administration warned this week. As a result ...
Eau Claire Leader-Telegram3d
U.S. Food and Drug Administration Approves Orphan Drug Designation for Nexcella NXC-201 as a ...
U.S. market exclusivity after approval; Tax credits for qualified clinical testing; Waiver of the Prescription Drug User Fee (currently at almost $3 million for a new d ...
SCOTUSblog12d
Food and Drug Administration v. Alliance for Hippocratic Medicine
Issues: (1) Whether respondents have Article III standing to challenge the Food and Drug Administration’s 2016 and 2021 actions with respect to mifepristone’s ...
Yahoo22d
U.S. Food and Drug Administration is warning people to stop using two eye drop products
The U.S. Food and Drug Administration is warning people to stop using two more eye drop products after the agency found bacterial contamination in some of them. According to a notice posted on the ...
The Bakersfield Californian3d
U.S. Food and Drug Administration Approves Orphan Drug Designation for Immix Biopharma NXC-201 ...
announced today that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) designation for NXC-201 for the treatment of a life-threatening blood disorder, Amyloid Light ...