Title 21 U.S.C. — Food and Drugs
757 sections
- § 1 — Repealed. June 25, 1938, ch. 675, § 1002(a), formerly § 902(a), 52 Stat. 1059; renumbered § 1002(a), Pub. L. 111–31, div. A, title I, § 101(b)(2), June 22, 2009, 123 Stat. 1784
- § 6 — Transferred
- § 7 — Repealed. June 25, 1938, ch. 675, § 1002(a), formerly § 902(a), 52 Stat. 1059; renumbered § 1002(a), Pub. L. 111–31, div. A, title I, § 101(b)(2), June 22, 2009, 123 Stat. 1784
- § 14a — Transferred
- § 15 — Repealed. June 25, 1938, ch. 675, § 1002(a), formerly § 902(a), 52 Stat. 1059; renumbered § 1002(a), Pub. L. 111–31, div. A, title I, § 101(b)(2), June 22, 2009, 123 Stat. 1784
- § 16 — Introduction into, or sale in, State or Territory or District of Columbia of dairy or food products falsely labeled or branded
- § 17 — Penalty for sale or introduction of falsely labeled dairy or food products; venue
- § 18 — Suspension of importation of adulterated articles
- § 19 — Repealed. May 29, 1928, ch. 901, § 1(100), 45 Stat. 993
- § 20 — Apples in interstate commerce; standard grades
- § 21 — Branding grades on barrels of apples
- § 22 — Barrels misbranded
- § 23 — Penalties
- § 24 — Omitted
- § 25 — Oleomargarine, butterine, or imitation butter or cheese transported into a State subject to its police powers
- § 26 — Omitted
- § 41 — Repealed. Pub. L. 104–128, § 2, Apr. 9, 1996, 110 Stat. 1198
- § 61 — Definitions
- § 62 — Manufacture, shipment, or delivery for shipment in interstate or foreign commerce prohibited
- § 63 — Penalties; acts of agents deemed acts of principals
- § 64 — Regulations for enforcement
- § 71 — Transferred
- § 93 — Repealed. May 29, 1928, ch. 901, § 1(92), 45 Stat. 993
- § 94 — Transferred
- § 96 — Repealed. Pub. L. 90–201, § 18, Dec. 15, 1967, 81 Stat. 600
- § 97 — Omitted
- § 98 — Transferred
- § 99 — Repealed. July 28, 1953, ch. 251, title I, § 101, 67 Stat. 208
- § 101 — Suspension of importation of all animals
- § 102 — Repealed. Pub. L. 107–171, title X, § 10418(a)(6), May 13, 2002, 116 Stat. 507
- § 106, — Omitted
- § 111, — Repealed. Pub. L. 107–171, title X, § 10418(a)(7), (8), May 13, 2002, 116 Stat. 507, 508
- § 112a — Omitted
- § 113 — Repealed. Pub. L. 107–171, title X, § 10418(a)(7), (8), May 13, 2002, 116 Stat. 507, 508
- § 113a — Establishment of research laboratories for foot-and-mouth disease and other animal diseases; research contracts; employment of technicians and scientists; appropriations
- § 114 — Repealed. Pub. L. 107–171, title X, § 10418(a)(8), (9), May 13, 2002, 116 Stat. 508
- § 114d–2 — Repealed. Pub. L. 92–152, § 3, Nov. 5, 1971, 85 Stat. 419
- § 114e — Repealed. Pub. L. 107–171, title X, § 10418(a)(10), (11), May 13, 2002, 116 Stat. 508
- § 114i — Pseudorabies eradication
- § 115 — Repealed. Pub. L. 107–171, title X, § 10418(a)(7), (8), (12)–(14), May 13, 2002, 116 Stat. 507, 508
- § 129 — Omitted
- § 129a — Repealed. Pub. L. 107–171, title X, § 10418(a)(1), (8), (16), May 13, 2002, 116 Stat. 507, 508
- § 132 — Transferred
- § 133 — Repealed. July 13, 1949, ch. 307, 63 Stat. 410
- § 134 — Repealed. Pub. L. 107–171, title X, § 10418(a)(17), (18), May 13, 2002, 116 Stat. 508
- § 136 — Additional inspection services
- § 136a — Collection of fees for inspection services
- § 141 — Prohibition of importation without permit
- § 142 — Milk or cream when unfit for importation
- § 143 — Inspection; certified statement in lieu thereof; waiver of requirements of section 142; regulations; suspension and revocation of permits
- § 144 — Unlawful receiving of imported milk or cream
- § 145 — Penalties
- § 146 — Authorization of appropriations
- § 147 — Repeal of inconsistent laws
- § 148 — Powers of State with respect to milk or cream lawfully imported
- § 149 — Definitions
- § 151 — Preparation and sale of worthless or harmful products for domestic animals prohibited; preparation to be in compliance with rules at licensed establishments
- § 152 — Importation regulated and prohibited
- § 153 — Inspection of imports; denial of entry and destruction
- § 154 — Regulations for preparation and sale; licenses
- § 154a — Special licenses for special circumstances; expedited procedure; conditions; exemptions; criteria
- § 155 — Permits for importation
- § 156 — Licenses conditioned on permitting inspection; suspension of licenses
- § 157 — Inspection
- § 158 — Offenses; punishment
- § 159 — Enforcement; penalties applicable; Congressional findings
- § 161 — Omitted
- § 171 — Repealed. Pub. L. 91–513, title III, § 1101(a)(2), (4), Oct. 27, 1970, 84 Stat. 1291
- § 175 — Repealed. June 27, 1952, ch. 477, title IV, § 403(a)(10), 66 Stat. 279
- § 176 — Repealed. Pub. L. 91–513, title III, § 1101(a)(2), (9), Oct. 27, 1970, 84 Stat. 1291, 1292
- § 186, — Transferred
- § 188 — Repealed. Pub. L. 91–513, title III, § 1101(a)(7), Oct. 27, 1970, 84 Stat. 1292
- § 191 — Repealed. Pub. L. 91–513, title III, § 1101(a)(1), Oct. 27, 1970, 84 Stat. 1291
- § 196 — Repealed. July 1, 1944, ch. 373, title XIII, § 1313, 58 Stat. 714
- § 197, — Repealed. Pub. L. 91–513, title III, § 1101(a)(4), Oct. 27, 1970, 84 Stat. 1291
- § 198a — Transferred
- § 199 — Repealed. Pub. L. 91–513, title III, § 1101(a)(5), Oct. 27, 1970, 84 Stat. 1292
- § 200 — Repealed. Nov. 2, 1951, ch. 666, § 5(2), 65 Stat. 769
- § 201 — Doing business without a license unlawful; employment of Chinese subjects
- § 202 — Certain classes of persons and corporations excepted; insecticides
- § 203 — Application for license; requirements; qualifications for license
- § 204 — Issuance of license
- § 205 — Display of license in pharmacy
- § 206 — Revocation of license
- § 207 — Restrictions on sales; written orders or prescriptions
- § 208 — Certain preparations and sales excepted
- § 209 — Poisons; book entry of sale; labels
- § 210 — Pharmacist; unauthorized use of title
- § 211 — Preservation of originals of prescriptions compounded and copies thereof; inspection of prescriptions by consular officers; marking containers of drugs
- § 212 — Offenses; punishment; duty to enforce provisions
- § 213 — Fraudulent representations to evade or defeat restrictions
- § 214 — Previous laws unaffected
- § 215 — “Consul” defined
- § 221 — Repealed. July 1, 1944, ch. 373, title XIII, § 1313, 58 Stat. 714
- § 301 — Short title
- § 321 — Definitions; generally
- § 321a — “Butter” defined
- § 321b — “Package” defined
- § 321c — Nonfat dry milk; “milk” defined
- § 321d — Market names for catfish and ginseng
- § 331 — Prohibited acts
- § 332 — Injunction proceedings
- § 333 — Penalties
- § 333a — Repealed. Pub. L. 101–647, title XIX, § 1905, Nov. 29, 1990, 104 Stat. 4853
- § 334 — Seizure
- § 335 — Hearing before report of criminal violation
- § 335a — Debarment, temporary denial of approval, and suspension
- § 335b — Civil penalties
- § 335c — Authority to withdraw approval of abbreviated drug applications
- § 336 — Report of minor violations
- § 337 — Proceedings in name of United States; provision as to subpoenas
- § 337a — Extraterritorial jurisdiction
- § 341 — Definitions and standards for food
- § 342 — Adulterated food
- § 343 — Misbranded food
- § 343–1 — National uniform nutrition labeling
- § 343–2 — Dietary supplement labeling exemptions
- § 343–3 — Disclosure
- § 343a — Repealed. Pub. L. 106–554, § 1(a)(1) [title V, § 517], Dec. 21, 2000, 114 Stat. 2763, 2763A–73
- § 344 — Emergency permit control
- § 345 — Regulations making exemptions
- § 346 — Tolerances for poisonous or deleterious substances in food; regulations
- § 346a — Tolerances and exemptions for pesticide chemical residues
- § 346b — Authorization of appropriations
- § 347 — Intrastate sales of colored oleomargarine
- § 347a — Congressional declaration of policy regarding oleomargarine sales
- § 347b — Contravention of State laws
- § 348 — Food additives
- § 349 — Bottled drinking water standards; publication in Federal Register
- § 350 — Vitamins and minerals
- § 350a — Infant formulas
- § 350a–1 — Protecting infants and improving formula supply
- § 350b — New dietary ingredients
- § 350c — Maintenance and inspection of records
- § 350d — Registration of food facilities
- § 350e — Sanitary transportation practices
- § 350f — Reportable food registry
- § 350g — Hazard analysis and risk-based preventive controls
- § 350h — Standards for produce safety
- § 350i — Protection against intentional adulteration
- § 350j — Targeting of inspection resources for domestic facilities, foreign facilities, and ports of entry; annual report
- § 350k — Laboratory accreditation for analyses of foods
- § 350l — Mandatory recall authority
- § 350l–1 — Annual report to Congress
- § 350m — Requirements for critical food
- § 351 — Adulterated drugs and devices
- § 352 — Misbranded drugs and devices
- § 353 — Exemptions and consideration for certain drugs, devices, and biological products
- § 353a — Pharmacy compounding
- § 353a–1 — Enhanced communication
- § 353b — Outsourcing facilities
- § 353c — Prereview of television advertisements
- § 353d — Process to update labeling for certain generic drugs
- § 354 — Veterinary feed directive drugs
- § 355 — New drugs
- § 355–1 — Risk evaluation and mitigation strategies
- § 355–2 — Actions for delays of generic drugs and biosimilar biological products
- § 355a — Pediatric studies of drugs
- § 355b — Adverse-event reporting
- § 355c — Research into pediatric uses for drugs and biological products
- § 355c–1 — Report
- § 355d — Internal committee for review of pediatric plans, assessments, deferrals, deferral extensions, and waivers
- § 355e — Pharmaceutical security
- § 355f — Extension of exclusivity period for new qualified infectious disease products
- § 355g — Utilizing real world evidence
- § 355h — Regulation of certain nonprescription drugs that are marketed without an approved drug application
- § 356 — Expedited approval of drugs for serious or life-threatening diseases or conditions
- § 356–1 — Accelerated approval of priority countermeasures
- § 356–2 — Accelerated approval Council
- § 356a — Manufacturing changes
- § 356b — Reports of postmarketing studies
- § 356c — Discontinuance or interruption in the production of life-saving drugs
- § 356c–1 — Annual reporting on drug shortages
- § 356d — Coordination; task force and strategic plan
- § 356e — Drug shortage list
- § 356f — Hospital repackaging of drugs in shortage
- § 356g — Standards for regenerative medicine and regenerative advanced therapies
- § 356h — Competitive generic therapies
- § 356i — Prompt reports of marketing status
- § 356j — Discontinuance or interruption in the production of medical devices
- § 356k — Platform technologies
- § 356l — Advanced manufacturing technologies designation program
- § 357 — Qualification of drug development tools
- § 358 — Authority to designate official names
- § 359 — Nonapplicability of subchapter to cosmetics
- § 360 — Registration of producers of drugs or devices
- § 360a — Clinical trial guidance for antibiotic drugs
- § 360a–1 — Clinical trials
- § 360a–2 — Susceptibility test interpretive criteria for microorganisms
- § 360aa — Recommendations for investigations of drugs for rare diseases or conditions
- § 360aaa — Omitted
- § 360b — New animal drugs
- § 360b–1 — Priority zoonotic animal drugs
- § 360bb — Designation of drugs for rare diseases or conditions
- § 360bbb — Expanded access to unapproved therapies and diagnostics
- § 360bbb–0 — Expanded access policy required for investigational drugs
- § 360bbb–0a — Investigational drugs for use by eligible patients
- § 360bbb–1 — Dispute resolution
- § 360bbb–2 — Classification of products
- § 360bbb–3 — Authorization for medical products for use in emergencies
- § 360bbb–3a — Emergency use of medical products
- § 360bbb–3b — Products held for emergency use
- § 360bbb–3c — Expedited development and review of medical products for emergency uses
- § 360bbb–4 — Countermeasure development, review, and technical assistance
- § 360bbb–4a — Priority review to encourage treatments for agents that present national security threats
- § 360bbb–4b — Medical countermeasure master files
- § 360bbb–5 — Critical Path Public-Private Partnerships
- § 360bbb–5a — Emerging technology program
- § 360bbb–6 — Risk communication
- § 360bbb–7 — Notification
- § 360bbb–8 — Consultation with external experts on rare diseases, targeted therapies, and genetic targeting of treatments
- § 360bbb–8a — Optimizing global clinical trials
- § 360bbb–8b — Use of clinical investigation data from outside the United States
- § 360bbb–8c — Patient participation in medical product discussion
- § 360bbb–8d — Notification, nondistribution, and recall of controlled substances
- § 360c — Classification of devices intended for human use
- § 360c–1 — Reporting
- § 360cc — Protection for drugs for rare diseases or conditions
- § 360ccc — Conditional approval of new animal drugs for minor use and minor species and certain new animal drugs
- § 360ccc–1 — Index of legally marketed unapproved new animal drugs for minor species
- § 360ccc–2 — Designated new animal drugs for minor use or minor species
- § 360d — Performance standards
- § 360dd — Open protocols for investigations of drugs for rare diseases or conditions
- § 360ddd — Definitions
- § 360ddd–1 — Regulation of medical gases
- § 360ddd–2 — Inapplicability of drug fees to designated medical gases
- § 360e — Premarket approval
- § 360e–1 — Pediatric uses of devices
- § 360e–3 — Breakthrough devices
- § 360e–4 — Predetermined change control plans for devices
- § 360ee — Grants and contracts for development of drugs for rare diseases and conditions
- § 360ee–1 — FDA rare neurodegenerative disease grant program
- § 360eee — Definitions
- § 360eee–1 — Requirements
- § 360eee–2 — National standards for prescription drug wholesale distributors
- § 360eee–3 — National standards for third-party logistics providers
- § 360eee–4 — Uniform national policy
- § 360f — Banned devices
- § 360ff — Priority review to encourage treatments for rare pediatric diseases
- § 360ff–1 — Targeted drugs for rare diseases
- § 360fff — Definitions
- § 360fff–1 — Submission of requests
- § 360fff–2 — Eligibility determinations; data submission; filing
- § 360fff–3 — GRASE determination
- § 360fff–4 — Guidance; other provisions
- § 360fff–5 — Repealed. Pub. L. 116–136, div. A, title III, § 3854(b)(5), Mar. 27, 2020, 134 Stat. 456
- § 360fff–6 — Non-sunscreen time and extent applications
- § 360fff–7 — Report
- § 360fff–8 — Sunset
- § 360g — Judicial review
- § 360g–1 — Agency documentation and review of significant decisions regarding devices
- § 360g–2 — Third party data transparency
- § 360h — Notification and other remedies
- § 360h–1 — Program to improve the device recall system
- § 360hh — Definitions
- § 360i — Records and reports on devices
- § 360ii — Program of control
- § 360j — General provisions respecting control of devices intended for human use
- § 360jj — Studies by Secretary
- § 360k — State and local requirements respecting devices
- § 360kk — Performance standards for electronic products
- § 360l — Postmarket surveillance
- § 360ll — Notification of defects in and repair or replacement of electronic products
- § 360m — Accredited persons
- § 360mm — Imports
- § 360n — Priority review to encourage treatments for tropical diseases
- § 360n–1 — Priority review for qualified infectious disease products
- § 360n–2 — Ensuring cybersecurity of devices
- § 360nn — Inspection, records, and reports
- § 360oo — Prohibited acts
- § 360pp — Enforcement
- § 360qq — Repealed. Pub. L. 105–362, title VI, § 601(a)(2)(A), Nov. 10, 1998, 112 Stat. 3285
- § 360rr — Federal-State cooperation
- § 360ss — State standards
- § 361 — Adulterated cosmetics
- § 362 — Misbranded cosmetics
- § 363 — Regulations making exemptions
- § 364 — Definitions
- § 364a — Adverse events
- § 364b — Good manufacturing practice
- § 364c — Registration and product listing
- § 364d — Safety substantiation
- § 364e — Labeling
- § 364f — Records
- § 364g — Mandatory recall authority
- § 364h — Small businesses
- § 364i — Exemption for certain products and facilities
- § 364j — Preemption
- § 371 — Regulations and hearings
- § 372 — Examinations and investigations
- § 372a — Transferred
- § 373 — Records
- § 374 — Inspection
- § 374a — Inspections relating to food allergens
- § 375 — Publicity
- § 376 — Examination of sea food on request of packer; marking food with results; fees; penalties
- § 377 — Revision of United States Pharmacopoeia; development of analysis and mechanical and physical tests
- § 378 — Advertising of foods
- § 379 — Confidential information
- § 379a — Presumption of existence of jurisdiction
- § 379aa — Serious adverse event reporting for nonprescription drugs
- § 379aa–1 — Serious adverse event reporting for dietary supplements
- § 379b — Consolidated administrative and laboratory facility
- § 379c — Transferred
- § 379d — Automation of Food and Drug Administration
- § 379d–1 — Conflicts of interest
- § 379d–2 — Policy on the review and clearance of scientific articles published by FDA employees
- § 379d–3 — Streamlined hiring authority
- § 379d–3a — Hiring authority for scientific, technical, and professional personnel
- § 379d–3b — Strategic Workforce Plan and report
- § 379d–4 — Reporting requirements
- § 379d–5 — Guidance document regarding product promotion using the Internet
- § 379dd — Establishment and functions of the Foundation
- § 379dd–1 — Location of Foundation
- § 379dd–2 — Activities of the Food and Drug Administration
- § 379e — Listing and certification of color additives for foods, drugs, devices, and cosmetics
- § 379f — Recovery and retention of fees for freedom of information requests
- § 379g — Definitions
- § 379h — Authority to assess and use drug fees
- § 379h–1 — Fees relating to advisory review of prescription-drug television advertising
- § 379h–2 — Reauthorization; reporting requirements
- § 379i — Definitions
- § 379j — Authority to assess and use device fees
- § 379j–1 — Reauthorization; reporting requirements
- § 379j–11 — Definitions
- § 379j–12 — Authority to assess and use animal drug fees
- § 379j–13 — Reauthorization; reporting requirements
- § 379j–21 — Authority to assess and use generic new animal drug fees
- § 379j–22 — Reauthorization; reporting requirements
- § 379j–31 — Authority to collect and use fees
- § 379j–41 — Definitions
- § 379j–42 — Authority to assess and use human generic drug fees
- § 379j–43 — Reauthorization; reporting requirements
- § 379j–51 — Definitions
- § 379j–52 — Authority to assess and use biosimilar biological product fees
- § 379j–53 — Reauthorization; reporting requirements
- § 379j–61 — Definitions
- § 379j–62 — Authority to assess and use outsourcing facility fees
- § 379j–71 — Definitions
- § 379j–72 — Authority to assess and use OTC monograph fees
- § 379j–73 — Reauthorization; reporting requirements
- § 379k — Information system
- § 379k–1 — Electronic format for submissions
- § 379l — Education
- § 379o — Environmental impact
- § 379r — National uniformity for nonprescription drugs
- § 379s — Preemption for labeling or packaging of cosmetics
- § 379v — Safety report disclaimers
- § 381 — Imports and exports
- § 382 — Exports of certain unapproved products
- § 383 — Office of International Relations
- § 384 — Importation of prescription drugs
- § 384a — Foreign supplier verification program
- § 384b — Voluntary qualified importer program
- § 384c — Inspection of foreign food facilities
- § 384d — Accreditation of third-party auditors
- § 384e — Recognition of foreign government inspections
- § 384f — Strengthening FDA and CBP coordination and capacity
- § 384g — Restricting entrance of illicit drugs
- § 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
- § 387v — Reporting on tobacco regulation activities
- § 391 — Separability clause
- § 392 — Exemption of meats and meat food products
- § 393 — Food and Drug Administration
- § 393a — Office of Pediatric Therapeutics
- § 394 — Scientific review groups
- § 395 — Loan repayment program
- § 396 — Practice of medicine
- § 397 — Contracts for expert review
- § 398 — Notices to States regarding imported food
- § 399 — Grants to enhance food safety
- § 399a — Office of the Chief Scientist
- § 399b — Office of Women’s Health
- § 399c — Improving the training of State, local, territorial, and tribal food safety officials
- § 399d — Employee protections
- § 399e — Nanotechnology
- § 399f — Ensuring adequate information regarding pharmaceuticals for all populations, particularly underrepresented subpopulations, including racial subgroups
- § 399g — Food and Drug Administration Intercenter Institutes
- § 399h — National Centers of Excellence in Advanced and Continuous Pharmaceutical Manufacturing
- § 399i — Food and Drug Administration Working Capital Fund
- § 399j — Abraham Accords Office
- § 451 — Congressional statement of findings
- § 452 — Congressional declaration of policy
- § 453 — Definitions
- § 454 — Federal and State cooperation in development and administration of State poultry product inspection programs
- § 455 — Inspection in official establishments
- § 456 — Operation of premises, facilities and equipment
- § 457 — Labeling and container standards
- § 458 — Prohibited acts
- § 459 — Compliance by all establishments
- § 460 — Miscellaneous activities subject to regulation
- § 461 — Offenses and punishment
- § 462 — Reporting of violations; notice; opportunity to present views
- § 463 — Rules and regulations
- § 464 — Exemptions
- § 465 — Limitations upon entry of poultry products and other materials into official establishments
- § 466 — Imports
- § 467 — Inspection services
- § 467a — Administrative detention; duration; pending judicial proceedings; notification of government authorities; release; removal of official marks
- § 467b — Seizure and condemnation
- § 467c — Federal court jurisdiction of enforcement and injunction proceedings and other kinds of cases; limitations; United States as plaintiff; subpenas
- § 467d — Administration and enforcement; applicability of penalty provisions; conduct of inquiries; power and jurisdiction of courts
- § 467e — Non-Federal jurisdiction of federally regulated matters; prohibition of additional or different requirements for establishments with inspection services and as to marking, labeling, packaging, and ingredients; recordkeeping and related requirements; concurrent jurisdiction over distribution for human food purposes of adulterated or misbranded and imported articles; other matters
- § 467f — Federal Food, Drug, and Cosmetic Act applications
- § 468 — Cost of inspection; overtime
- § 469 — Authorization of appropriations
- § 470 — Omitted
- § 471 — Safe Meat and Poultry Inspection Panel
- § 472 — Interstate shipment of poultry inspected by Federal and State agencies for certain small establishments
- § 473 — Grants for improvements to meat and poultry facilities to allow for interstate shipment
- § 501 — Repealed. Pub. L. 91–513, title III, § 1101(a)(10), Oct. 27, 1970, 84 Stat. 1292
- § 601 — Definitions
- § 602 — Congressional statement of findings
- § 603 — Examination of animals prior to slaughter; use of humane methods
- § 604 — Post mortem examination of carcasses and marking or labeling; destruction of carcasses condemned; reinspection
- § 605 — Examination of carcasses brought into slaughtering or packing establishments, and of meat food products issued from and returned thereto; conditions for entry
- § 606 — Inspection and labeling of meat food products
- § 607 — Labeling, marking, and container requirements
- § 608 — Sanitary inspection and regulation of slaughtering and packing establishments; rejection of adulterated meat or meat food products
- § 609 — Examination of animals and food products thereof, slaughtered and prepared during nighttime
- § 610 — Prohibited acts
- § 611 — Devices, marks, labels, and certificates; simulations
- § 612 — Notification
- § 613 — Plans and reassessments
- § 614 — Repealed. Pub. L. 107–171, title X, § 10418(a)(19), May 13, 2002, 116 Stat. 508
- § 615 — Inspection of carcasses, meat of which is intended for export
- § 616 — Inspectors of carcasses, etc., meat of which is intended for export; certificates of condition
- § 617 — Clearance prohibited to vessel carrying meat for export without inspector’s certificate
- § 618 — Delivery of inspectors’ certificates, and of copies
- § 619 — Marking, labeling, or other identification to show kinds of animals from which derived; separate establishments for preparation and slaughtering activities
- § 620 — Imports
- § 621 — Inspectors to make examinations provided for; appointment; duties; regulations
- § 622 — Bribery of or gifts to inspectors or other officers and acceptance of gifts
- § 623 — Exemptions from inspection requirements
- § 624 — Storage and handling regulations; violations; exemption of establishments subject to non-Federal jurisdiction
- § 625 — Inapplicability of certain requirements to catfish
- § 626 — Purchase of tags, labels, stamps, and certificates
- § 641 — Prohibition of subchapter I inspection of articles not intended for use as human food; denaturation or other identification prior to distribution in commerce; inedible articles
- § 642 — Recordkeeping requirements
- § 643 — Registration of business, name of person, and trade names
- § 644 — Regulation of transactions, transportation, or importation of 4–D animals to prevent use as human food
- § 645 — Federal provisions applicable to State or Territorial business transactions of a local nature and not subject to local authority
- § 661 — Federal and State cooperation
- § 671 — Inspection services; refusal or withdrawal; hearing; business unfitness based upon certain convictions; other provisions for withdrawal of services unaffected; responsible connection with business; finality of Secretary’s actions; judicial review; record
- § 672 — Administrative detention; duration; pending judicial proceedings; notification of governmental authorities; release
- § 673 — Seizure and condemnation
- § 674 — Federal court jurisdiction of enforcement and injunction proceedings and other kinds of cases; limitations of section 607(e) of this title
- § 675 — Assaulting, resisting, or impeding certain persons; murder; protection of such persons
- § 676 — Violations
- § 677 — Other Federal laws applicable for administration and enforcement of chapter; location of inquiries; jurisdiction of Federal courts
- § 678 — Non-Federal jurisdiction of federally regulated matters; prohibition of additional or different requirements for establishments with inspection services and as to marking, labeling, packaging, and ingredients; recordkeeping and related requirements; concurrent jurisdiction over distribution for human food purposes of adulterated or misbranded and imported articles; other matters
- § 679 — Application of Federal Food, Drug, and Cosmetic Act
- § 679a — Safe Meat and Poultry Inspection Panel
- § 679b — Pasteurization of meat and poultry
- § 679c — Expansion of Food Safety Inspection Service activities
- § 680 — Authorization of appropriations
- § 683 — Interstate shipment of meat inspected by Federal and State agencies for certain small establishments
- § 691 — Omitted
- § 692 — Inspection extended to reindeer
- § 693 — Inspection of dairy products for export
- § 694 — Authorization of appropriations
- § 695 — Payment of cost of meat-inspection service; exception
- § 801 — Congressional findings and declarations: controlled substances
- § 801a — Congressional findings and declarations: psychotropic substances
- § 802 — Definitions
- § 803 — Repealed. Pub. L. 95–137, § 1(b), Oct. 18, 1977, 91 Stat. 1169
- § 811 — Authority and criteria for classification of substances
- § 812 — Schedules of controlled substances
- § 813 — Treatment of controlled substance analogues
- § 814 — Removal of exemption of certain drugs
- § 821 — Rules and regulations
- § 822 — Persons required to register
- § 822a — Prescription drug take back expansion
- § 823 — Registration requirements
- § 824 — Denial, revocation, or suspension of registration
- § 825 — Labeling and packaging
- § 826 — Production quotas for controlled substances
- § 826a — Attorney General report on drug shortages
- § 827 — Records and reports of registrants
- § 828 — Order forms
- § 829 — Prescriptions
- § 829a — Delivery of a controlled substance by a pharmacy to an administering practitioner
- § 830 — Regulation of listed chemicals and certain machines
- § 831 — Additional requirements relating to online pharmacies and telemedicine
- § 832 — Suspicious orders
- § 841 — Prohibited acts A
- § 842 — Prohibited acts B
- § 843 — Prohibited acts C
- § 844 — Penalties for simple possession
- § 844a — Civil penalty for possession of small amounts of certain controlled substances
- § 845 — Transferred
- § 846 — Attempt and conspiracy
- § 847 — Additional penalties
- § 848 — Continuing criminal enterprise
- § 849 — Transportation safety offenses
- § 850 — Information for sentencing
- § 851 — Proceedings to establish prior convictions
- § 852 — Application of treaties and other international agreements
- § 853 — Criminal forfeitures
- § 853a — Transferred
- § 854 — Investment of illicit drug profits
- § 855 — Alternative fine
- § 856 — Maintaining drug-involved premises
- § 857 — Repealed. Pub. L. 101–647, title XXIV, § 2401(d), Nov. 29, 1990, 104 Stat. 4859
- § 858 — Endangering human life while illegally manufacturing controlled substance
- § 859 — Distribution to persons under age twenty-one
- § 860 — Distribution or manufacturing in or near schools and colleges
- § 860a — Consecutive sentence for manufacturing or distributing, or possessing with intent to manufacture or distribute, methamphetamine on premises where children are present or reside
- § 861 — Employment or use of persons under 18 years of age in drug operations
- § 862 — Denial of Federal benefits to drug traffickers and possessors
- § 862a — Denial of assistance and benefits for certain drug-related convictions
- § 862b — Sanctioning for testing positive for controlled substances
- § 863 — Drug paraphernalia
- § 864 — Anhydrous ammonia
- § 864a — Grants to reduce production of methamphetamines from anhydrous ammonia
- § 865 — Smuggling methamphetamine or methamphetamine precursor chemicals into the United States while using facilitated entry programs
- § 871 — Attorney General
- § 871a — Semiannual reports to Congress
- § 872 — Education and research programs of Attorney General
- § 872a — Public-private education program
- § 873 — Cooperative arrangements
- § 874 — Advisory committees
- § 875 — Administrative hearings
- § 876 — Subpenas
- § 877 — Judicial review
- § 878 — Powers of enforcement personnel
- § 879 — Search warrants
- § 880 — Administrative inspections and warrants
- § 881 — Forfeitures
- § 881–1, — Transferred
- § 882 — Injunctions
- § 883 — Enforcement proceedings
- § 884 — Immunity and privilege
- § 885 — Burden of proof; liabilities
- § 886 — Payments and advances
- § 886a — Diversion Control Fee Account
- § 887 — Coordination and consolidation of post-seizure administration
- § 888 — Repealed. Pub. L. 106–185, § 2(c)(3), Apr. 25, 2000, 114 Stat. 210
- § 889 — Production control of controlled substances
- § 890 — Review of Federal sales of chemicals usable to manufacture controlled substances
- § 901 — Severability
- § 902 — Savings provisions
- § 903 — Application of State law
- § 904 — Payment of tort claims
- § 951 — Definitions
- § 952 — Importation of controlled substances
- § 953 — Exportation of controlled substances
- § 954 — Transshipment and in-transit shipment of controlled substances
- § 955 — Possession on board vessels, etc., arriving in or departing from United States
- § 955a — Transferred
- § 956 — Exemption authority
- § 957 — Persons required to register
- § 958 — Registration requirements
- § 959 — Possession, manufacture, or distribution of controlled substance
- § 960 — Prohibited acts A
- § 960a — Foreign terrorist organizations, terrorist persons and groups
- § 961 — Prohibited acts B
- § 962 — Second or subsequent offenses
- § 963 — Attempt and conspiracy
- § 964 — Additional penalties
- § 965 — Applicability of part E of subchapter I
- § 966 — Authority of Secretary of the Treasury
- § 967 — Smuggling of controlled substances; investigations; oaths; subpenas; witnesses; evidence; production of records; territorial limits; fees and mileage of witnesses
- § 968 — Service of subpena; proof of service
- § 969 — Contempt proceedings
- § 970 — Criminal forfeitures
- § 971 — Notification, suspension of shipment, and penalties with respect to importation and exportation of listed chemicals
- § 1001 — Repealed. Pub. L. 97–35, title V, § 587(a)(3), Aug. 13, 1981, 95 Stat. 480
- § 1031 — Congressional statement of findings
- § 1032 — Congressional declaration of policy
- § 1033 — Definitions
- § 1034 — Inspection of egg products
- § 1035 — Sanitary operating practices in official plants
- § 1036 — Pasteurization and labeling of egg products at official plants
- § 1037 — Prohibited acts
- § 1038 — Cooperation with appropriate State and other governmental agencies; utilization of employees; reimbursement
- § 1039 — Eggs and egg products not intended for use as human food; inspection; denaturing or otherwise identifying
- § 1040 — Recordkeeping requirements; persons required to maintain records; scope of disclosure; access to records
- § 1041 — Enforcement provisions
- § 1042 — Reporting of violation to United States attorney for institution of criminal proceedings; procedure; presentation of views
- § 1043 — Rules and regulations; administration and enforcement
- § 1044 — Exemption of certain activities
- § 1045 — Limitation on entry of eggs and egg products and other materials into official plants
- § 1046 — Imports
- § 1047 — Refusal or withdrawal of inspection services; hearing; grounds; person deemed to have responsible connection with business; finality of order of Secretary; judicial review; other provisions for refusal of services unaffected
- § 1048 — Administrative detention of violative articles; duration; release; removal of official marks
- § 1049 — Seizure and condemnation proceedings
- § 1050 — Jurisdiction of district courts; United States as plaintiff in enforcement and restraining proceedings; subpenas for witnesses
- § 1051 — Other Federal laws applicable for administration and enforcement of chapter; prosecution of inquiries; exercise of jurisdiction
- § 1052 — State or local regulation
- § 1053 — Inspection and administration costs
- § 1054 — Annual report to Congressional committees
- § 1055 — Authorization of appropriations
- § 1056 — Separability
- § 1101 — Congressional findings
- § 1102 — Congressional declaration of national policy
- § 1103 — Repealed. Pub. L. 100–690, title I, § 1007(c)(1), Nov. 18, 1988, 102 Stat. 4187
- § 1104 — Repealed. Pub. L. 94–237, § 4(c)(1), Mar. 19, 1976, 90 Stat. 244
- § 1111 — Repealed. Pub. L. 100–690, title I, § 1007(c)(1), Nov. 18, 1988, 102 Stat. 4187
- § 1115 — Notice relating to the control of dangerous drugs
- § 1116 — Repealed. Pub. L. 100–690, title I, § 1007(c)(1), Nov. 18, 1988, 102 Stat. 4187
- § 1117 — Repealed. Pub. L. 98–24, § 4(b), Apr. 26, 1983, 97 Stat. 183
- § 1118 — Omitted
- § 1121 — Repealed. Pub. L. 92–255, title I, § 104, Mar. 21, 1972, 86 Stat. 67
- § 1131 — Omitted
- § 1134 — Repealed. Pub. L. 92–255, title I, § 104, Mar. 21, 1972, 86 Stat. 67
- § 1151 — Repealed. Pub. L. 92–255, title I, § 104, Mar. 21, 1972, 86 Stat. 67
- § 1161 — Repealed. Pub. L. 98–509, title III, § 301(d), Oct. 19, 1984, 98 Stat. 2364
- § 1171 — Drug abuse prevention function appropriations
- § 1172 — Repealed. Pub. L. 98–24, § 2(c)(2), Apr. 26, 1983, 97 Stat. 182
- § 1173 — Transferred and Omitted
- § 1174, — Transferred
- § 1176 — Repealed. Pub. L. 97–35, title IX, § 969(a), Aug. 13, 1981, 95 Stat. 595
- § 1177 — Special project grants and contracts
- § 1178 — Records and audit
- § 1179 — National Drug Abuse Training Center
- § 1180 — Transferred
- § 1181 — Contract authority
- § 1191 — Transferred
- § 1194 — Repealed. Pub. L. 98–24, § 2(c)(2), Apr. 26, 1983, 97 Stat. 182
- § 1201 — Repealed. Pub. L. 100–690, title I, § 1007(a)(3), Nov. 18, 1988, 102 Stat. 4187
- § 1301 — Omitted
- § 1401 — Pesticide monitoring and enforcement information
- § 1402 — Foreign pesticide information
- § 1403 — Pesticide analytical methods
- § 1501, — Repealed. Pub. L. 100–690, title I, § 1009, Nov. 18, 1988, 102 Stat. 4188, as amended by Pub. L. 105–20, § 2(b), June 27, 1997, 111 Stat. 234
- § 1502a — Transferred
- § 1503 — Repealed. Pub. L. 100–690, title I, § 1009, Nov. 18, 1988, 102 Stat. 4188, as amended by Pub. L. 105–20, § 2(b), June 27, 1997, 111 Stat. 234
- § 1505a — Annual report on development and deployment of narcotics detection technologies
- § 1506 — Repealed. Pub. L. 100–690, title I, § 1009, Nov. 18, 1988, 102 Stat. 4188, as amended by Pub. L. 105–20, § 2(b), June 27, 1997, 111 Stat. 234; Pub. L. 115–271, title VIII, § 8203(a)(3), Oct. 24, 2018, 132 Stat. 4111; Pub. L. 116–74, § 2(c)(1)(A)(i)(III), Nov. 27, 2019, 133 Stat. 1157
- § 1509 — Repealed. Pub. L. 109–469, title XI, § 1101(b), Dec. 29, 2006, 120 Stat. 3539
- § 1521 — Findings
- § 1522 — Purposes
- § 1523 — Definitions
- § 1524 — Authorization of appropriations
- § 1531 — Establishment of drug-free communities support program
- § 1532 — Program authorization
- § 1533 — Information collection and dissemination with respect to grant recipients
- § 1534 — Technical assistance and training
- § 1535 — Supplemental grants for coalition mentoring activities
- § 1536 — Community-based coalition enhancement grants to address local drug crises
- § 1541 — Repealed. Pub. L. 115–271, title VIII, § 8203(b)(5), Oct. 24, 2018, 132 Stat. 4112; Pub. L. 116–74, § 2(c)(1)(A)(ii)(II), Nov. 27, 2019, 133 Stat. 1157
- § 1601 — Findings
- § 1602 — Definitions
- § 1603 — General requirements; applicability; preemption
- § 1604 — Liability of biomaterials suppliers
- § 1605 — Procedures for dismissal of civil actions against biomaterials suppliers
- § 1606 — Subsequent impleader of dismissed biomaterials supplier
- § 1701 — Definitions
- § 1702 — Office of National Drug Control Policy
- § 1703 — Appointment and duties of Director and Deputy Directors
- § 1704 — Coordination with National Drug Control Program agencies in demand reduction, supply reduction, and State and local affairs
- § 1705 — Development, submission, implementation, and assessment of National Drug Control Strategy
- § 1706 — High Intensity Drug Trafficking Areas Program
- § 1707 — Repealed. Pub. L. 115–271, title VIII, § 8222(3), Oct. 24, 2018, 132 Stat. 4143
- § 1708 — Emerging Threats Committee, plan, and media campaign
- § 1708a — Repealed. Pub. L. 116–74, § 2(b)(1), Nov. 27, 2019, 133 Stat. 1157
- § 1709 — Repealed. Pub. L. 109–469, title XI, § 1101(a), Dec. 29, 2006, 120 Stat. 3539
- § 1710 — Drug Interdiction Coordinator and Committee
- § 1710a — Requirement for disclosure of Federal sponsorship of all Federal advertising or other communication materials
- § 1711 — Authorization of appropriations
- § 1712 — Repealed. Pub. L. 115–271, title VIII, § 8202(b)(2), Oct. 24, 2018, 132 Stat. 4110
- § 1713 — Authorization of use of environmentally-approved herbicides to eliminate illicit narcotics crops
- § 1714 — Awards for demonstration programs by local partnerships to coerce abstinence in chronic hard-drug users under community supervision through the use of drug testing and sanctions
- § 1715 — GAO audit
- § 1801 — Repealed. Pub. L. 109–469, title V, § 501(b), Dec. 29, 2006, 120 Stat. 3533
- § 1901 — Findings and policy
- § 1902 — Purpose
- § 1903 — Public identification of significant foreign narcotics traffickers and required reports
- § 1904 — Blocking assets and prohibiting transactions
- § 1905 — Authorities
- § 1906 — Enforcement
- § 1907 — Definitions
- § 1908 — Judicial Review Commission on Foreign Asset Control
- § 2001 — Designation of United States Anti-Doping Agency
- § 2002 — Records, audit, and report
- § 2003 — Authorization of appropriations
- § 2004 — Information sharing
- § 2011 — Definitions
- § 2012 — Establishment of clearinghouse and advisory council
- § 2013 — NMIC requirements and review
- § 2014 — Authorization of appropriations
- § 2101 — Findings
- § 2102 — Ensuring the safety of pet food
- § 2103 — Ensuring efficient and effective communications during a recall
- § 2104 — State and Federal cooperation
- § 2105 — Enhanced aquaculture and seafood inspection
- § 2106 — Consultation regarding genetically engineered seafood products
- § 2107 — Sense of Congress
- § 2108 — Annual report to Congress
- § 2109 — Publication of annual reports
- § 2110 — Rule of construction
- § 2201 — Performance standards
- § 2202 — National Agriculture and Food Defense Strategy
- § 2203 — Food and Agriculture Coordinating Councils
- § 2204 — Building domestic capacity
- § 2205 — Food allergy and anaphylaxis management
- § 2206 — Alcohol-related facilities
- § 2221 — Food emergency response network
- § 2222 — Integrated consortium of laboratory networks
- § 2223 — Enhancing tracking and tracing of food and recordkeeping
- § 2224 — Surveillance
- § 2225 — Decontamination and disposal standards and plans
- § 2241 — Inspection by the Secretary of Commerce
- § 2242 — Foreign offices of the Food and Drug Administration
- § 2243 — Smuggled food
- § 2251 — Jurisdiction; authorities
- § 2252 — Compliance with international agreements
- § 2301 — Sense of Congress
- § 2302 — Definitions
- § 2311 — Identification of foreign opioid traffickers
- § 2312 — Imposition of sanctions
- § 2313 — Description of sanctions
- § 2313a — Designation of transactions of sanctioned persons as of primary money laundering concern
- § 2314 — Waivers
- § 2315 — Procedures for judicial review of classified information
- § 2316 — Briefings on implementation
- § 2331 — Director of National Intelligence program on use of intelligence resources in efforts to sanction foreign opioid traffickers
- § 2332 — Authorization of appropriations
- § 2333 — Regulatory authority
- § 2334 — Termination
- § 2335 — Exception relating to importation of goods
- § 2341 — Definitions
- § 2351 — Finding; policy
- § 2352 — Use of national emergency authorities; reporting
- § 2353 — Imposition of sanctions with respect to fentanyl trafficking by transnational criminal organizations
- § 2354 — Penalties; waivers; exceptions
- § 2355 — Treatment of forfeited property of transnational criminal organizations
- § 2361 — Treatment of transnational criminal organizations in suspicious transactions reports of the Financial Crimes Enforcement Network
- § 2371 — Exception relating to importation of goods
- § 2401 — Definitions
- § 2402 — Major international doping fraud conspiracies
- § 2403 — Criminal penalties and statute of limitations
- § 2404 — Coordination and sharing of information with USADA