State Codes and Statutes

Statutes > Virginia > Title-54-1 > Chapter-34 > 54-1-3413

§ 54.1-3413. Manufacturing and administering Schedule I drugs.

It shall be lawful for a person to manufacture, and for a practitioner toadminister, Schedule I drugs if:

1. The manufacturer and practitioner are expressly authorized to engage insuch activities by the Attorney General of the United States, or pursuant tothe federal Food, Drug and Cosmetic Act;

2. The manufacturer or dispenser is registered under all appropriateprovisions of this chapter;

3. Any Schedule I drug so manufactured is sold or furnished on an officialwritten order to a practitioner or other authorized person only; and

4. The manufacturer and practitioner comply with all other requirements ofthis chapter.

(1970, c. 650, § 54-524.58:1; 1972, c. 798; 1988, c. 765.)

State Codes and Statutes

Statutes > Virginia > Title-54-1 > Chapter-34 > 54-1-3413

§ 54.1-3413. Manufacturing and administering Schedule I drugs.

It shall be lawful for a person to manufacture, and for a practitioner toadminister, Schedule I drugs if:

1. The manufacturer and practitioner are expressly authorized to engage insuch activities by the Attorney General of the United States, or pursuant tothe federal Food, Drug and Cosmetic Act;

2. The manufacturer or dispenser is registered under all appropriateprovisions of this chapter;

3. Any Schedule I drug so manufactured is sold or furnished on an officialwritten order to a practitioner or other authorized person only; and

4. The manufacturer and practitioner comply with all other requirements ofthis chapter.

(1970, c. 650, § 54-524.58:1; 1972, c. 798; 1988, c. 765.)


State Codes and Statutes

State Codes and Statutes

Statutes > Virginia > Title-54-1 > Chapter-34 > 54-1-3413

§ 54.1-3413. Manufacturing and administering Schedule I drugs.

It shall be lawful for a person to manufacture, and for a practitioner toadminister, Schedule I drugs if:

1. The manufacturer and practitioner are expressly authorized to engage insuch activities by the Attorney General of the United States, or pursuant tothe federal Food, Drug and Cosmetic Act;

2. The manufacturer or dispenser is registered under all appropriateprovisions of this chapter;

3. Any Schedule I drug so manufactured is sold or furnished on an officialwritten order to a practitioner or other authorized person only; and

4. The manufacturer and practitioner comply with all other requirements ofthis chapter.

(1970, c. 650, § 54-524.58:1; 1972, c. 798; 1988, c. 765.)