Department of Health and Human Services November 7, 2006 – Federal Register Recent Federal Regulation Documents

Program Exclusions: October 2006
Document Number: E6-18758
Type: Notice
Date: 2006-11-07
Agency: Department of Health and Human Services, Office of Inspector General, Inspector General Office, Health and Human Services Department, Centers for Medicare & Medicaid Services
Proposed Data Collections Submitted for Public Comment and Recommendations
Document Number: E6-18746
Type: Notice
Date: 2006-11-07
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Agency Forms Undergoing Paperwork Reduction Act Review
Document Number: E6-18744
Type: Notice
Date: 2006-11-07
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Agency Forms Undergoing Paperwork Reduction Act Review
Document Number: E6-18741
Type: Notice
Date: 2006-11-07
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Oral Dosage Form New Animal Drugs; Ivermectin, Pyrantel, and Praziquantel Tablets
Document Number: E6-18684
Type: Rule
Date: 2006-11-07
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of an original new animal drug application (NADA) filed by Virbac AH, Inc. The NADA provides for veterinary prescription use of chewable tablets in dogs containing ivermectin, pyrantel pamoate, and praziquantel for the treatment and control or prevention of various internal parasites.
New Animal Drugs for Use in Animal Feeds; Bambermycins
Document Number: E6-18680
Type: Rule
Date: 2006-11-07
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is amending the animal drug regulations to correct an inadvertent error in the conditions of use of bambermycins free-choice cattle feeds. This action is being taken to improve the accuracy of the animal drug regulations.
Implantation or Injectable Dosage Form New Animal Drugs; Lincomycin; Correction
Document Number: E6-18679
Type: Rule
Date: 2006-11-07
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is correcting a document amending the animal drug regulations to reflect approval of an abbreviated new animal drug application (ANADA) that appeared in the Federal Register of September 1, 2006 (71 FR 51995). FDA is correcting the date of approval of an ANADA for a generic lincomycin injectable solution which was drafted in error. This correction is being made to improve the accuracy of the Federal Register.
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.