In this episode, Keller and Heckman Partner Azim Chowdhury returns to the podcast to discuss FDA’s evolving regulation of tobacco and nicotine products, with a focus on flavored vaping products, e-cigarettes, and oral nicotine pouches. Azim provides updates and insights on PMTA authorizations and the legal standards companies must satisfy to bring products to market. Join us as we explore recent litigation, new FDA guidance, and landmark authorization decisions that may shape the future of flavored ENDS and nicotine pouches in the United States.