Department of Health and Human Services December 7, 2007 – Federal Register Recent Federal Regulation Documents

Implantation or Injectable Dosage Form New Animal Drugs; Erythromycin
Document Number: E7-23763
Type: Rule
Date: 2007-12-07
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 a supplemental new animal drug application (NADA) filed by Cross Vetpharm Group Ltd. The supplemental NADA provides for use of a 100 milligram per milliliter (mg/mL) strength erythromycin injectable solution in cattle for the treatment of bovine respiratory disease.
Agency Information Collection Activities: Submission for OMB Review; Comment Request
Document Number: E7-23746
Type: Notice
Date: 2007-12-07
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
National Heart, Lung, and Blood Institute; Notice of Closed Meeting
Document Number: 07-5970
Type: Notice
Date: 2007-12-07
Agency: Department of Health and Human Services, National Institutes of Health
Proposed Information Collection Activity; Comment Request
Document Number: 07-5965
Type: Notice
Date: 2007-12-07
Agency: Department of Health and Human Services, Administration for Children and Families, Children and Families Administration
Proposed Information Collection Activity; Comment Request
Document Number: 07-5964
Type: Notice
Date: 2007-12-07
Agency: Department of Health and Human Services, Administration for Children and Families, Children and Families Administration
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.