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19814 Federal Register / Vol. 79, No. 69 / Thursday, April 10, 2014 / Rules and Regulations 292 73 2105, Version B, dated December 16, 2010, which are not incorporated by reference in this AD, can
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How to fill out new animal drugs for:

01
Gather all necessary information, such as the animal's species and age, the specific drug being administered, and any relevant medical history.
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Follow the instructions provided by the drug manufacturer or veterinarian on the drug's label or prescription. This may include dosage instructions, frequency of administration, and any additional precautions.
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Ensure accurate record-keeping by documenting each administration of the drug, including the date, time, dosage, and any observed reactions or side effects.
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Dispose of any unused or expired medications properly, following local regulations and guidelines.

Who needs new animal drugs for:

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Pet owners who have pets that require medication for various health conditions, such as infections, allergies, or chronic illnesses.
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Livestock farmers who need to treat specific diseases or manage the health of their animals.
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Veterinary professionals who prescribe and administer drugs for animals in their care, including veterinarians, veterinary technicians, and veterinary pharmacists.
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New animal drugs are used for the treatment, prevention, or control of animal diseases or conditions.
Manufacturers or sponsors of new animal drugs are required to file for approval with the appropriate regulatory agency.
New animal drugs must be filled out with all relevant information about the drug, including indications, dosages, side effects, etc.
The purpose of new animal drugs is to ensure the safety and efficacy of medications used in veterinary medicine.
Information such as active ingredients, intended use, safety data, and manufacturing process must be reported on new animal drugs.
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