[Federal Register: February 26, 1999 (Volume 64, Number 38)]
[Notices]               
[Page 9515]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr26fe99-76]


[[Page 9515]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration
[Docket No. 93N-0371]

 
Agency Information Collection Activities; Announcement of OMB 
Approval; Prescription Drug Product Labeling, Medication Guide 
Requirements

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 ``Prescription Drug Product 
Labeling, Medication Guide Requirements'' has been approved by the 
Office of Management and Budget (OMB) under the Paperwork Reduction Act 
of 1995.

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 1, 1998 
(63 FR 66378), 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 0910-0393. 
The approval expires on January 31, 2002.

    Dated: February 19, 1999.
 William K. Hubbard,
 Associate Commissioner for Policy Coordination.
[FR Doc. 99-4765 Filed 2-25-99; 8:45 am]
BILLING CODE 4160-01-F