Between October 2023 and September 2024, USFDA had granted 694 approvals for Abbreviated New Drug Application (ANDA), allowing applicants to manufacture and market the generic drug for America.
A New York state lawmaker is proposing a ban on the sale of what he described as "highly addictive" flavored nicotine pouches, even after the U.S. Food and Drug Administration came out in support ...
Co-Diagnostics withdrew its application to the Food and Drug Administration for a Covid-19 test. The Salt Lake City diagnostics company said Friday it plans to submit an enhanced version of the ...
Feb 21 (Reuters) - The U.S. Food and Drug Administration said on Friday there was no longer a shortage of Novo Nordisk's NOVOb.CO popular weight-loss and diabetes drugs, Wegovy and ...
The deal with Breckenridge Pharmaceutical, Inc., a subsidiary of Towa International, includes the USFDA-approved Abbreviated New Drug Application (ANDA) for 250 mcg and 500 mcg tablets.
List of more than two dozen "prohibited words" circulates at FDA White House says list may have misinterpreted Trump gender order White House says FDA should prohibit some of the words on list Feb ...
The US Food and Drug Administration (FDA) has granted priority review to Boehringer Ingelheim’s new drug application (NDA) for zongertinib to treat unresectable or metastatic non-small cell lung ...
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