State Codes and Statutes

Statutes > Virginia > Title-54-1 > Chapter-34 > 54-1-3421

§ 54.1-3421. New drugs.

A. No person shall sell, deliver, offer for sale, hold for sale or give awayany new drug unless an application with respect to the drug has been approvedand the approval has not been withdrawn under § 505 of the federal Food,Drug, and Cosmetic Act (21 U.S.C. § 355).

B. This section shall not apply to a drug subject to the federal act intendedsolely for investigational use and for which a notice of claimedinvestigational exemption for a new drug has been filed with the U.S. Foodand Drug Administration in accordance with 21 C.F.R. Part 312.

(1970, c. 650, § 54-524.95; 1988, c. 765; 2000, c. 135.)

State Codes and Statutes

Statutes > Virginia > Title-54-1 > Chapter-34 > 54-1-3421

§ 54.1-3421. New drugs.

A. No person shall sell, deliver, offer for sale, hold for sale or give awayany new drug unless an application with respect to the drug has been approvedand the approval has not been withdrawn under § 505 of the federal Food,Drug, and Cosmetic Act (21 U.S.C. § 355).

B. This section shall not apply to a drug subject to the federal act intendedsolely for investigational use and for which a notice of claimedinvestigational exemption for a new drug has been filed with the U.S. Foodand Drug Administration in accordance with 21 C.F.R. Part 312.

(1970, c. 650, § 54-524.95; 1988, c. 765; 2000, c. 135.)


State Codes and Statutes

State Codes and Statutes

Statutes > Virginia > Title-54-1 > Chapter-34 > 54-1-3421

§ 54.1-3421. New drugs.

A. No person shall sell, deliver, offer for sale, hold for sale or give awayany new drug unless an application with respect to the drug has been approvedand the approval has not been withdrawn under § 505 of the federal Food,Drug, and Cosmetic Act (21 U.S.C. § 355).

B. This section shall not apply to a drug subject to the federal act intendedsolely for investigational use and for which a notice of claimedinvestigational exemption for a new drug has been filed with the U.S. Foodand Drug Administration in accordance with 21 C.F.R. Part 312.

(1970, c. 650, § 54-524.95; 1988, c. 765; 2000, c. 135.)