Food additive petitions: Reporting and recordkeeping requirements,

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Federal Register: June 15, 1998 (Volume 63, Number 114)NoticesPage 32673From the Federal Register Online via GPO Access [wais.access.gpo.gov]

DOCID:fr15jn98-56

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

Docket No. 97N-0487Agency Information Collection Activities; Announcement of OMB Approval

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

SUMMARY: The Food and Drug Administration (FDA) is announcing that a collection of information entitled ``Abbreviated New Drug Application Regulations, Patent and Exclusivity Provision'' has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (the PRA).

FOR FURTHER INFORMATION CONTACT: Karen L. Nelson, Office of Information Resources Management (HFA-250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-1482.

SUPPLEMENTARY INFORMATION: In the Federal Register of December 12, 1997 (62 FR 65431), the agency announced that the proposed information collection had been submitted to OMB for review and clearance under section 3507 of the PRA (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 0910-0305. The approval expires on May 31, 2001.

Dated: June 5, 1998. William K. Hubbard, Associate Commissioner for Policy Coordination.

FR Doc. 98-15768Filed6-12-98; 8:45 amBILLING CODE 4160-01-F

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