United States Government Publishing Office publisher pbl distributor dst United States National Archives and Records Administration Office of the Federal Register author aut Government Organization text government publication eng FR Regulatory Information 2011_register executive 2011-03-29 article Rules and Regulations D09002ee1c800244d D09002ee1c800253e United States Department of Health and Human Services originator org United States Government Agency or Subagency United States Food and Drug Administration originator org United States Government Agency or Subagency The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect revised human food safety warnings or updated pathogen nomenclature on dosage form new animal drug product labeling that have not been codified. The regulations are also being amended to correct the wording of certain other conditions of use, to correct minor errors, and to revise some sections to reflect a current format. These actions are being taken to comply with the Federal Food, Drug, and Cosmetic Act (FD&C Act) and to improve the accuracy and readability of the regulations. 76 FR 17336 https://www.govinfo.gov/app/details/FR-2011-03-29/2011-7313 2011-7313 fr29mr11-4 4160-01-P Docket No. FDA-2011-N-0003 https://www.govinfo.gov/app/details/FR-2011-03-29/2011-7313 https://www.govinfo.gov/content/pkg/FR-2011-03-29/html/2011-7313.htm https://www.govinfo.gov/content/pkg/FR-2011-03-29/pdf/2011-7313.pdf 4 p. 17336 17339 76 FR 17336 Title 21 Part 520 21 CFR Part 520 Title 21 Part 522 21 CFR Part 522 Title 21 Part 526 21 CFR Part 526 Title 21 Part 529 21 CFR Part 529 New Animal Drugs; Amikacin Sulfate, Ampicillin Trihydrate, Ceftiofur Hydrochloride, Cephapirin Benzathine, Chlortetracycline, Fenbendazole, Formalin, Furosemide, Glucose/Glycine/Electrolyte, Pyrantel Pamoate, Sulfadimethoxine, Sulfamethazine, and Tetracycline; Federal Register Vol. 76, Issue RULE 2011-7313 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 2011-03-29 Docket No. FDA-2011-N-0003 4160-01-P 2011-7313 Final rule; correcting amendments.

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect revised human food safety warnings or updated pathogen nomenclature on dosage form new animal drug product labeling that have not been codified. The regulations are also being amended to correct the wording of certain other conditions of use, to correct minor errors, and to revise some sections to reflect a current format. These actions are being taken to comply with the Federal Food, Drug, and Cosmetic Act (FD&C Act) and to improve the accuracy and readability of the regulations.

This rule is effective March 29, 2011. George K. Haibel, Center for Veterinary Medicine (HFV-6), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-276-9019, e-mail: george.haibel@fda.hhs.gov. New Animal Drugs: Amikacin Sulfate, Ampicillin Trihydrate, Ceftiofur Hydrochloride, Cephapirin Benzathine, etc.; Correcting Amendments , george.haibel@fda.hhs.gov Vol. 76, no. 60 Office of the Federal Register, National Archives and Records Administration 2011-03-29 continuing daily deposited born digital 205 p. Table of Contents: AE 2.7: GS 4.107: AE 2.106: KF70.A2 https://www.govinfo.gov/app/details/FR-2011-03-29 P0b002ee180c94d60 0097-6326 0042-1219 0364-1406 769-004-00000-9 000582072 f:fr29mr11 https://www.govinfo.gov/app/details/FR-2011-03-29 https://www.govinfo.gov/content/pkg/FR-2011-03-29/pdf/FR-2011-03-29.pdf https://www.govinfo.gov/content/pkg/FR-2011-03-29/xml/FR-2011-03-29.xml fdlp 17327 17520 DGPO 2011-03-29 2024-06-04 FR-2011-03-29 machine generated eng FR FR-2011-03-29 76 60