99-17332. Agency Information Collection Activities; Announcement of OMB Approval; Current Good Manufacturing Practice Regulations for Finished Pharmaceuticals

[Federal Register Volume 64, Number 130 (Thursday, July 8, 1999)]
[Notices]
[Pages 36884-36885]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-17332]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration
[Docket No. 98N-1110]


Agency Information Collection Activities; Announcement of OMB 
Approval; Current Good Manufacturing Practice Regulations for Finished 
Pharmaceuticals

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``CGMP Regulations for Finished 
Pharmaceuticals'' 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 April 19, 1999 
(64 FR 19180), 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 0910-0139. 
The approval expires on June 30, 2002. A copy of the supporting 
statement for this information collection is available on the Internet 
at ``http://www.fda.gov/ohrms/dockets''.


[[Page 36885]]


    Dated: June 30, 1999.
Margaret M. Dotzel,
Acting Associate Commissioner for Policy Coordination.
[FR Doc. 99-17332 Filed 7-7-99; 8:45 am]
BILLING CODE 4160-01-F