It shall be lawful for a person to manufacture, and for a practitioner to administer, Schedule I drugs if:\n1. The manufacturer and practitioner are expressly authorized to engage in such activities by the Attorney General of the United States, or pursuant to the federal Food, Drug and Cosmetic Act;\n2. The manufacturer or dispenser is registered under all appropriate provisions of this chapter;\n3. Any Schedule I drug so manufactured is sold or furnished on an official written order to a practitioner or other authorized person only; and\n4. The manufacturer and practitioner comply with all other requirements of this chapter.\n1970, c. 650, § 54-524.58:1; 1972, c. 798; 1988, c. 765.
Virginia Legal Code