Department of Health and Human Services March 24, 2011 – Federal Register Recent Federal Regulation Documents

Announcement of an Award
Document Number: 2011-6991
Type: Notice
Date: 2011-03-24
Agency: Department of Health and Human Services, Administration for Children and Families
The Administration for Children and Families (ACF), Office of the Deputy Assistant Secretary and Inter-Departmental Liaison for Early Childhood Development announces the award of a cooperative agreement with the Congressional Hunger Center (CHC) in Washington, DC, to work with ACF programs on hunger and obesity issues for young children. An award in the amount of $3,000 has been made to the CHC.
National Heart, Lung, and Blood Institute; Notice of Closed Meetings
Document Number: 2011-6967
Type: Notice
Date: 2011-03-24
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meeting
Document Number: 2011-6966
Type: Notice
Date: 2011-03-24
Agency: Department of Health and Human Services, National Institutes of Health
Submission for OMB Review; Comment Request
Document Number: 2011-6947
Type: Notice
Date: 2011-03-24
Agency: Department of Health and Human Services, Administration for Children and Families
Agency Forms Undergoing Paperwork Reduction Act Review
Document Number: 2011-6936
Type: Notice
Date: 2011-03-24
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
New Animal Drugs; Change of Sponsor's Name and Address; Corrections
Document Number: 2011-6795
Type: Rule
Date: 2011-03-24
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) published a document in the Federal Register of April 20, 2010 (75 FR 20522) amending the animal drug regulations to reflect changes to a sponsor's name and address. That document contained errors in the regulatory text. FDA is correcting the tables listing sponsors of approved animal drug applications (NADAs) by adding a change to the sponsor's drug labeler code (DLC). Cross-references to the sponsor's DLC are amended in two sections of the Code of Federal Regulations (CFR) containing the conditions of use approved animal drug products. These corrections are being made to improve the accuracy of the animal drug regulations.
Certain Other Dosage Form New Animal Drugs; Detomidine; Correction
Document Number: 2011-6791
Type: Rule
Date: 2011-03-24
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) published a document in the Federal Register of April 23, 2010 (75 FR 21162), that amended the animal drug regulations to reflect approval of an original new animal drug application (NADA). FDA is correcting a paragraph describing limitations to the approved conditions of use for detomidine hydrochloride oromucosal gel in horses. This correction is being made to improve the accuracy of the animal drug regulations.
Animal Drugs, Feeds, and Related Products; Withdrawal of Approval of New Animal Drug Applications; Aklomide; Levamisole Hydrochloride; Nitromide and Sulfanitran; Roxarsone; Correction
Document Number: 2011-6790
Type: Rule
Date: 2011-03-24
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) published a document in the Federal Register of October 26, 2010 (75 FR 65565) amending the animal drug regulations. The October 26, 2010, final rule amended the regulations by removing those portions that reflect approval of eight new animal drug applications. The final rule inadvertently failed to add conforming amendments in Sec. 558.530. FDA is correcting the animal drug regulations by removing cross references for use of the withdrawn drugs in combination drug medicated feed. This correction is being made to improve the accuracy of the animal drug regulations.
New Animal Drugs for Use in Animal Feeds; Florfenicol; Correction
Document Number: 2011-6789
Type: Rule
Date: 2011-03-24
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) published a document in the Federal Register of June 17, 2010 (75 FR 34361) revising the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA). That document contained an incorrect table entry describing the maximum florfenicol concentration in Type B medicated swine feeds. This correction is being made to improve the accuracy of the animal drug regulations.
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