On This Page Date: July 25 – 26, 2024 Day1: Thu, Jul 25 11:00 AM – 3:00 PM ET Day2: Fri, Jul 26 11:00 AM – […]

Image Español The U.S. Food and Drug Administration wants consumers to know certain “wellness” vaping products containing vitamins and/or essential oils are being illegally sold with […]

Get this high-resolution graphic on Flickr. Español Americans spend a lot of money on creams, lotions and other cosmetics that promise to improve their skin, hair, […]

Export requirements apply to investigational new drugs (INDs) as follows: Exporting Investigational New Drugs to a Listed CountrySection 802(c) of the Federal Food Drug and Cosmetic […]

Drugs made in the U.S. are not always approved by FDA but may be approved by regulatory authorities in other countries. Exporters must comply with U.S. […]

FDA works to help assure safe and quality drugs are exported from the U.S. for use around the world. The agency reviews thousands of electronic certificate […]

Who Is the Audience for This Website? FDA’s generic drug-specific labeling resources are primarily directed to industry staff who develop generic drug labeling. For more information […]

This page is intended to assist industry when making certain regulatory submissions in electronic format to the FDA’s Adverse Event Reporting System (FAERS) database for the […]

This list contains GDUFA facility payments received by the Agency. The following table explains the terms used in the list: Column Description Fiscal Year The Fiscal Year […]