[Federal Register Volume 85, Number 179 (Tuesday, September 15, 2020)]
[Notices]
[Pages 57220-57221]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-20332]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2013-N-0618, FDA-2010-N-0601, FDA-2010-N-0598, FDA-
2013-N-1155, FDA-2010-N-0118, FDA-2020-N-0145, FDA-2010-N-0597, FDA-
2014-N-0086, FDA-2016-N-2836, FDA-2019-N-5841, and FDA-2019-N-5973]


Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approvals

AGENCY: Food and Drug Administration, Health and Human Services (HHS).

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is publishing a list of 
information collections that have been approved by the Office of 
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Operations, 
Food and Drug Administration, Three White Flint North, 10A-12M, 11601 
Landsdown St., North Bethesda, MD 20852, 301-796-7726, 
[email protected].

SUPPLEMENTARY INFORMATION: The following is a list of FDA information 
collections recently approved by OMB under section 3507 of the 
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control 
number and expiration date of OMB approval for each information 
collection are shown in table 1. Copies of the supporting statements 
for the information collections are available on the internet at http://www.reginfo.gov/public/do/PRAMain. 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.

        Table 1--List of Information Collections Approved by OMB
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                                            OMB control    Date approval
           Title of collection                  No.           expires
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Reporting and Recordkeeping for                0910-0025       8/31/2023
 Electronic Products--General
 Requirements...........................
Current Good Manufacturing Practice            0910-0152       8/31/2023
 Regulations for Medicated Feed.........
Good Manufacturing Practice Regulations        0910-0154       8/31/2023
 for Type A Medicated Articles, 21 CFR
 Part 226...............................
Food Labeling Regulations...............       0910-0381       8/31/2023
Prior Notice of Imported Food Under the        0910-0520       8/31/2020
 Public Health Security and Bioterrorism
 Preparedness and Response Act of 2002..

[[Page 57221]]

 
Animal Drug User Fee Program............       0910-0540       8/31/2023
Index of Legally Marketed Unapproved New       0910-0620       8/31/2023
 Animal Drugs for Minor Species.........
Potential Tobacco Product Violations           0910-0716       8/31/2023
 Reporting Form.........................
Donor Risk Assessment Questionnaire for        0910-0841       8/31/2023
 the FDA/National Heart, Lung, and Blood
 Institute--Sponsored Transfusion-
 Transmissible Infections Monitoring
 System--Risk Factor Elicitation........
Generic Clearance for Qualitative Data         0910-0891       8/31/2023
 to Support Social and Behavioral
 Research for Food, Dietary Supplements,
 Cosmetics, and Animal Food and Feed....
Health Care Providers Understanding of         0910-0892       8/31/2023
 Opioid Analgesic Abuse-Deterrent
 Formulations: Phase 2 and 3 Surveys....
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    Dated: September 9, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-20332 Filed 9-14-20; 8:45 am]
BILLING CODE 4164-01-P