Final answer:
Veterinary drugs must have FDA-mandated labels detailing approved uses, routes, doses, and species. The Center for Veterinary Medicine regulates these standards to ensure safety and efficacy, manage environmental impacts, and conduct ongoing safety monitoring.
Step-by-step explanation:
Yes, veterinary drugs are required by the FDA to have labels that include important information such as approved uses, routes, doses, and the species for which the drug is intended. The Center for Veterinary Medicine (CVM) is a branch of the FDA that oversees these regulations. The labeling is crucial for ensuring that the drugs are used safely and effectively, preventing drug residues in food products from animals, and maintaining environmental safety by addressing concerns such as drug excretion into soil and water. For instance, the FDA has set requirements to prevent conditions like bovine spongiform encephalopathy, which are also administered by CVM through inspections of animal feed manufacturers. Plus, drugs must be advertised only for the conditions they are approved for, with a fair balance of benefits and risks, as per drug advertising regulations. It is also essential for drug companies to engage in postmarket safety surveillance even after the drug has been approved and is on the market.