FDA

Hims & Hers cancels its low-cost Wegovy knockoff pill after FDA threats and legal pressure, highlighting regulatory enforcement.

The Food and Drug Administration (FDA) announced that it has expanded the "no artificial colors" label to be used by companies and their products.

The Food and Drug Administration (FDA) is investigating whether COVID-19 vaccines are linked to adult deaths.

FDA Chief Medical Officer and Center for Biologics Evaluation and Research Director Vinay Prasad has called for the agency to reflect following reports that children's deaths are linked to the COVID-19 vaccine.

The Food and Drug Administration moved to limit the use of unapproved fluoride products for children, taking action to restrict their sale.

Tylenol manufacturer Kenvue Brands LLC sent a letter to the Food and Drug Administration, criticizing demands that the drug's label be changed to reflect greater safety warnings.

The FDA announced the first round of pharmaceuticals that will receive expedited reviews under the Commissioner’s National Priority Voucher (CNPV) pilot program.

The Food and Drug Administration approved a generic abortion pill.

Walmart announced that it will remove synthetic dyes from its products.

The Food and Drug Administration (FDA) announced that it has initiated the process of changing the labeling for Tylenol in light of President Trump's announcement that acetaminophen is linked to autism development when used during pregnancy.