21 U.S. Code Subchapter IX - TOBACCO PRODUCTS
- § 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
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.
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