0910-AG11 200904 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Revision of the Requirements for Publication of License Revocation Info./Admin./Other Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 601.8 15 USC 1451 to 1561 21 USC 321 21 USC 351 to 353 21 USC 355 21 USC 356b 21 USC 360 21 USC 360c to 360f 21 USC 360h to 360j 21 USC 371 21 USC 374 21 USC 379e 21 USC 381 42 USC 216 42 USC 241 42 USC 262 and 263 42 USC 264, sec 122 PL 105-115, 111 Stat. 2322 (21 USC 355 note) No NPRM-Companion to Direct Final Rule 06/00/2009 Direct Final Rule 06/00/2009 No No None No No No Paul Levine E. Jr. 0910 Food and Drug Administration FDA 301 827-6210 Center for Biologics Evaluation and Research, Suite 200N (HFM-17), 1401 Rockville Pike, Rockville MD 20852