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FDA is very concerned about the safety of products not approved for
parenteral use which are infused or injected into food producing
animals. FDA believes that the packaging and labeling of these products
is a subterfuge to avoid the more stringent regulatory requirements for
parenteral drugs. Products that are intended for oral or topical
administration should not be packaged to facilitate parenteral (injection,
udder infusion) administration. Such drugs will be considered to be
misbranded if they do not contain directions for their packaged use.































































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