§ 54.1-3413. Manufacturing and administering Schedule I drugs
It 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; and
4. 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.)
Sections: Previous 54.1-3409 54.1-3410 54.1-3410.1 54.1-3410.2 54.1-3411 54.1-3411.1 54.1-3412 54.1-3413 54.1-3414 54.1-3415 54.1-3416 54.1-3417 54.1-3418 54.1-3419 54.1-3420 NextLast modified: April 3, 2009