Section 54.1-3413 - Manufacturing and administering Schedule I drugsIt shall be lawful for a person to manufacture, and for a practitioner to administer, Schedule I drugs if:
1. 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;2. The manufacturer or dispenser is registered under all appropriate provisions of this chapter;3. Any Schedule I drug so manufactured is sold or furnished on an official written order to a practitioner or other authorized person only; and4. The manufacturer and practitioner comply with all other requirements of this chapter.1970, c. 650, § 54-524.58:1; 1972, c. 798; 1988, c. 765.Amended by Acts 1988, c. 765.Amended by Acts 1972, c. 798.Amended by Acts 1970, c. 650, § 54-524.58:1.