As used in § 5257 through § 5259 of this Article, “generic drug” means the chemical or generic name, as determined by the United States Adopted Names (USAN) and accepted by the Federal Food and Drug Administration (FDA), of those drug products having the same active chemical ingredients. SOURCE: GC § 6600.4 added by P.L. 16-040:1 (Sept. 26, 1981); P.L. 16-124:2 (Dec. 30, 1982) renumbered this section as GC § 6965.7. Codified by the Compiler as 5 GCA § 5269.