- § 387. Definitions
- § 387a. FDA authority over tobacco products
- § 387a–1. Final rule
- § 387b. Adulterated tobacco products
- § 387c. Misbranded tobacco products
- § 387d. Submission of health information to the Secretary
- § 387e. Annual registration
- § 387f. General provisions respecting control of tobacco products
- § 387f–1. Enforcement action plan for advertising and promotion restrictions
- § 387g. Tobacco product standards
- § 387h. Notification and other remedies
- § 387i. Records and reports on tobacco products
- § 387j. Application for review of certain tobacco products
- § 387k. Modified risk tobacco products
- § 387l. Judicial review
- § 387m. Equal treatment of retail outlets
- § 387n. Jurisdiction of and coordination with the Federal Trade Commission
- § 387o. Regulation requirement
- § 387p. Preservation of State and local authority
- § 387q. Tobacco Products Scientific Advisory Committee
- § 387r. Drug products used to treat tobacco dependence
- § 387s. User fees
- § 387t. Labeling, recordkeeping, records inspection
- § 387u. Studies of progress and effectiveness
21 U.S. Code SUBCHAPTER IX— TOBACCO PRODUCTS
Prior Provisions
A prior subchapter IX of this chapter, consisting of sections 391 to 399a of this title, was redesignated subchapter X by Pub. L. 111–31, div. A, title I, § 101(b)(1), June 22, 2009, 123 Stat. 1784.