Sen. Richard Durbin (D-IL) sent a letter on Oct. 16 to the U.S. Food and Drug Administration (FDA) urging the agency to publish a list of electronic nicotine delivery system (ENDS) products for which it has received a premarket tobacco product application (PMTA). Manufacturers of ENDS products were required to submit a PMTA to FDA by Sept. 9, 2020, to remain on the market. Without a publicly available list, retailers – including travel centers – will not know which products are legal for them to sell.
10-22-2020The U.S. Food and Drug Administration’s (FDA’s) Center for Tobacco Policy issued a statement on Aug. 31 indicating the agency plans to publish a list of electronic nicotine delivery system (ENDS) products for which it has received a premarket tobacco product application (PMTA). FDA’s announcement is a win for the travel center industry. Without a publicly available list, retailers – including travel centers – will not know which products are legal for them to sell.
08-31-2020ºÚÁÏÉçÇøjoined a letter to the U.S. Food and Drug Administration (FDA) on Aug. 25 urging the agency to publish a list of electronic nicotine delivery system (ENDS) products for which it has received a premarket tobacco product application (PMTA) by the Sept. 9, 2020, deadline. Without a publicly available list, retailers – including travel centers – will not know which products are legal for them to sell.
08-25-2020