0910-AG20 200904 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Amendment to the Current Good Manufacturing Practice Regulations for Finished Pharmaceuticals Substantive, Nonsignificant First Time Published in The Unified Agenda Proposed Rule Stage Undetermined Undetermined 21 CFR 210 21 CFR 211 21 USC 321 21 USC 351 21 USC 352 21 USC 355 21 USC 360b 21 USC 371 21 USC 374 42 USC 216 42 USC 262 42 USC 263a 42 USC 264 No NPRM 02/00/2010 Undetermined Businesses Undetermined No Undetermined No No Paula Katz 0910 Food and Drug Administration FDA 301 796-6972 301 847-8742 paula.katz@fda.hhs.gov Suite 3037 (HFD-7), Center for Drug Evaluation and Research, WO 51, Room 4314, 10903 New Hampshire Avenue, Silver Spring MD 20993