[Federal Register: August 10, 2007 (Volume 72, Number 154)] [Notices] [Page 45053-45054] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr10au07-95] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 2006N-0104] Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format AGENCY: Food and Drug Administration, HHS. ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (FDA) is announcing that a collection of information entitled ``Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format'' has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: Elizabeth Berbakos, Office of the Chief [[Page 45054]] Information Officer (HFA-250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-1482. SUPPLEMENTARY INFORMATION: In the Federal Register of December 13, 2006 (71 FR 74924), the agency announced that the proposed information collection had been submitted to OMB for review and clearance under 44 U.S.C. 3507. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910-0530. The approval expires on May 31, 2010. A copy of the supporting statement for this information collection is available on the Internet at http://www.fda.gov/ohrms/dockets. Dated: August 6, 2007. Jeffrey Shuren, Assistant Commissioner for Policy. [FR Doc. E7-15614 Filed 8-9-07; 8:45 am] BILLING CODE 4160-01-S