0910-AG18 200910 The Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Electronic Distribution of Content of Labeling for Human Prescription Drug and Biological Products Other Significant Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 201.100 21 CFR 201.306 21 CFR 201.310 21 USC 321 21 USC 331 21 USC 351 21 USC 352 21 USC 353 21 USC 355 21 USC 358 21 USC 360 21 USC 360b 21 USC 360gg - 360ss 21 USC 371 21 USC 374 21 USC 379e 42 USC 216 42 USC 241 42 USC 262 42 USC 264 No NPRM 03/00/2010 Undetermined None No No No No Ilisa Bernstein B. G. 0910 Food and Drug Administration FDA 301 796-4830 ilisa.bernstein@fda.hhs.gov Room 15-74 (HF-23), Office of Policy, WO1, Room 4341, 10903 New Hampshire Avenue, Silver Spring MD 20993