Treatments for dry eye disease, neuroendocrine tumors, chronic spontaneous urticaria, Barth syndrome, and migraine are under review.

Many of us assume that the US Food and Drug Administration ... or endorsement. Registration simply means the manufacturer has filed their info with the FDA—which is required by law.

Generic names are assigned by international organizations, such as the U.S. Adopted Names (USAN) Council, the Food and Drug Administration (FDA), or the World Health Organization (WHO), to ensure ...

In a statement, the FDA said it confirmed Novo Nordisk's "stated product availability and manufacturing capacity" of these prescription drugs meets or exceeds current and projected demand.

The FDA has set a PDUFA target action date of October 23, 2025, for the low-dose atropine formulation.

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 ...