0910-AA61 200304 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Investigational New Drugs: Export Requirements for Unapproved New Drug Products Routine and Frequent Previously Published in The Unified Agenda Final Rule Stage No No 21 CFR 312.110 21 USC 321 21 USC 381 21 USC 382 21 USC 393 42 USC 241 42 USC 243 42 USC 262 21 USC 331 21 USC 351 to 353 21 USC 355 21 USC 371 No NPRM 06/19/2002 67 FR 41642 Final Action 09/00/2003 No None No NA Not Collected Philip Chao L. 0910 Food and Drug Administration FDA 240 400-4053 philip.chao@fda.hhs.gov Room 15-61 (HF-23), Center for Food Safety and Applied Nutrition, 5001 Campus Drive, College Park MD 20740