0910-AB91 200310 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 Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format Other Significant Previously Published in The Unified Agenda Final Rule Stage No Private Sector 21 CFR 314 21 CFR 601 21 USC 321 21 USC 331 21 USC 351 21 USC 353 21 USC 355 21 USC 360 21 USC 371 21 USC 374 21 USC 379e 42 USC 262 ... No NPRM 05/03/2002 67 FR 22367 Final Action 12/00/2003 No Businesses Federal No NA Not Collected Darren Eicken 0910 Food and Drug Administration FDA 301 796-0978 301 827-8440 darren.eicken@fda.hhs.gov Room 3037, (HFD-7), Center for Drug Evaluation and Research, Building 51, Room 6206, 10903 New Hampshire Avenue, Silver Spring MD 20993-0002