0910-AG81 201404 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Requirements for the Submission of Data Needed to Calculate User Fees for Domestic Manufacturers and Importers of Tobacco Products Other Significant Previously Published in The Unified Agenda Final Rule Stage No No 21 CFR 1150 (new) 21 USC 371 21 USC 387s PL 111-31 No NPRM 05/31/2013 78 FR 32581 NPRM Comment Period End 08/14/2013 Final Action 06/00/2014 Yes Businesses None No No Yes No Annette Marthaler 0910 Food and Drug Administration FDA 240 753-3043 annette.marthaler@fda.hhs.gov Office of Combination Products, 10903 New Hampshire Avenue, WO32, Room 5129, Silver Spring MD 20993