Sec. 372. Misbranding
87 words·~1 min read·
/bill/116/hr/19/ih/section-372A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
Section 502 of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 352 ) is amended by adding at the end the following: If it is a nonprescription drug that is subject to section 505G, is not the subject of an application approved under section 505, and does not comply with the requirements under section 505G. If it is a drug and it was manufactured, prepared, propagated, compounded, or processed in a facility for which fees have not been paid as required by section 744M. .
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U.S. Code