21 CFR § 1107.48 Exemption Requests and Substantial Equivalence Reports

§ 1107.48 Issuance of an order denying marketing authorization.

Current through Sep 8, 2026 · Read all of Part 1107

(a) General. FDA will issue an order that the new tobacco product cannot be marketed if FDA finds that:

(1) The information submitted in the SE Report does not establish that the new tobacco product is substantially equivalent to a predicate tobacco product that was commercially marketed (other than for test marketing) in the United States on February 15, 2007; or

(2) The new tobacco product is not in compliance with the Federal Food, Drug, and Cosmetic Act.

(b) Basis for order. The order will describe the basis for denying marketing authorization.

← § 1107.46 Issuance of an order finding a new tobacco product substantially equivalent.§ 1107.50 Rescission of order. →