Peytant Solutions has received marketing authorisation from the US Food and Drug Administration (FDA) for its AMStent ...
The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the ...
It has been a very busy year for food recalls in the United States. The U.S. Food and Drug Administration (FDA) and the U.S.
The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries.
The U.S. Food and Drug Administration has approved Avadel Pharmaceuticals' sleep disorder drug for children aged 7 years and ...
Some patients fear tirzepatide, sold by Eli Lilly under the brand names Zepbound and Mounjaro, will be hard to get and prohibitively expensive once compounding pharmacies are no longer producing it.
This could be due to U.S. Food and Drug Administration recalls. The FDA has continued to suspend food and drug items that people might typically buy. Here is a list of September food and drug ...
On Thursday, the U.S. Food and Drug Administration (FDA) approved COBENFY (xanomeline and trospium chloride), an oral medication that is manufactured by Bristol Myers Squibb in New Jersey.
On October 2, 2024, the U.S. Food and Drug Administration (FDA) determined the shortage of the tirzepatide injection, a glucagon-like peptide ...
Passengers on 200 Delta flights were denied in-flight meal service after food safety issues were discovered in the airline's ...
Amid an ongoing pet food recall, the U.S. Food and Drug Administration (FDA) is urging pet owners not to give their dogs and ...
today announced that the U.S. Food and Drug Administration (FDA) has approved COBENFYâ„¢ (xanomeline and trospium chloride), an oral medication for the treatment of schizophrenia in adults.