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Nded as follows: DEPARTMENT OF THE TREASURY PART 510 NEW ANIMAL DRUGS 26 CFR Part 1 1. The authority citation for 21 CFR part 510 continues to read as follows: TD 9572 Internal Revenue Service Food and Drug Administration 21 CFR Parts 510 and 520 Docket No. FDA 2011 N 0003 Authority: 21 U.S.C. 321, 331, 351, 352, 353, 360b, 371, 379e. New Animal Drugs; Change of Sponsor; Chlortetracycline Powder AGENCY: Food and Drug Administration, HHS. ACTION: Final rule. The Food.
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Caa FAQ
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The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation.
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Animal Drugs In most cases, the Federal Food, Drug, and Cosmetic Act requires that an animal drug be approved by FDA before a drug sponsor can legally sell the drug.
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The U.S. Department of Agriculture (USDA) is authorized, under the 1913 Virus-Serum-Toxin Act as amended by the 1985 Food Security Act, to ensure that all veterinary biologics produced in, or imported into, the United States are not worthless, contaminated, dangerous, or harmful.
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An approved animal drug has gone through the New Animal Drug Application (NADA) process, or for an approved generic animal drug, the Abbreviated New Animal Drug Application (ANADA) process. If the information in the application meets the requirements for approval, FDA approves the animal drug.
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Commonly used medication types Examples in dogs and cats include , -sulfa, and . Non-steroidal anti-inflammatories: these common drugs reduce swelling, inflammation, pain and lameness.
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FDA's Center for Veterinary Medicine (CVM) approves and regulates new animal drugs.
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An approved animal drug has gone through FDA's drug approval process. During this process, the agency reviews information submitted by the drug company about the animal drug.
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Animal Drugs– The Federal Food, Drug, and Cosmetic Act gives FDA the legal authority to approve and regulate drugs for animals. Before a drug company can market an animal drug, the company must get the drug approved by FDA.
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