DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2011-N-0362] Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Current Good Manufacturing Practices for Finished Pharmaceuticals AGENCY:

Food and Drug Administration, HHS.

 ACTION:

Notice.

 SUMMARY:

The Food and Drug Administration (FDA) is announcing that a collection of information entitled “Current Good Manufacturing Practices for Finished Pharmaceuticals” has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.

 FOR FURTHER INFORMATION CONTACT:

FDA PRA Staff, Office of Operations, Food and Drug Administration, 8455 Colesville Rd., COLE-14526, Silver Spring, MD 20993-0002, PRAStaff@fda.hhs.gov.

SUPPLEMENTARY INFORMATION:

On March 06, 2015, the Agency submitted a proposed collection of information entitled “Current Good Manufacturing Practices for Finished Pharmaceuticals” 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 0910-0139. The approval expires on May 31, 2018. A copy of the supporting statement for this information collection is available on the Internet at http://www.reginfo.gov/public/do/PRAMain.

Dated: June 1, 2015. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2015-13696 Filed 6-4-15; 8:45 am] BILLING CODE 4164-01-P