Act of June 25, 1938, ch. V, subch. G, sec. 575 (as amended)

DEFINITIONS.

Year: 2026Length: 230 wordsOfficial source
SEC. 575. [21 U.S.C. 360ddd] DEFINITIONS. In this subchapter: (1) The term “designated medical gas” means any of the following: (A) Oxygen that meets the standards set forth in an official compendium. (B) Nitrogen that meets the standards set forth in an official compendium. (C) Nitrous oxide that meets the standards set forth in an official compendium. (D) Carbon dioxide that meets the standards set forth in an official compendium. (E) Helium that meets the standards set forth in an official compendium. (F) Carbon monoxide that meets the standards set forth in an official compendium. (G) Medical air that meets the standards set forth in an official compendium. (H) Any other medical gas deemed appropriate by the Secretary, after taking into account any investigational new drug application or investigational new animal drug application for the same medical gas submitted in accordance with regulations applicable to such applications in title 21 of the Code of Federal Regulations, unless any period of exclusivity for a new drug under section 505(c)(3)(E)(ii) or section 505(j)(5)(F)(ii), or the extension of any such period under section 505A, or any period of exclusivity for a new animal drug under section 512(c)(2)(F), applicable to such medical gas has not expired. (2) The term “medical gas” means a drug that— (A) is manufactured or stored in a liquefied, nonliquefied, or cryogenic state; and (B) is administered as a gas.
Cross-references to the US Code
21 U.S.C. 360ddd
Act of June 25, 1938, ch. V, subch. G, sec. 575 (as amended): DEFINITIONS. | Justis AI