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21 U.S.C. § 1705 — Development, submission, implementation, and assessment of National Drug Control Strategy
Federal law — U.S. Code and appendices · legal_authorities
**(a) In general**
(1) **Statement of drug policy priorities** — The Director shall release a statement of drug control policy priorities in the calendar year of a Presidential inauguration following the inauguration, but not later than April 1.
(2) **National Drug Control Strategy submitted by the President** — Not later than the first Monday in February following the year in which the term of the President commences, and every 2 years thereafter, the President shall submit to Congress a National Drug Control Strategy.
**(b) Development of the National Drug Control Strategy**
(1) **Promulgation** — The Director shall promulgate the National Drug Control Strategy, which shall set forth a comprehensive plan to reduce illicit drug use and the consequences of such illicit drug use in the United States by limiting the availability of and reducing the demand for illegal drugs and promoting prevention, early intervention, treatment, and recovery support for individuals with substance use disorders.
(2) **State and local commitment** — The Director shall seek the support and commitment of State, local, and Tribal officials in the formulation and implementation of the National Drug Control Strategy.
(3) **Strategy based on evidence** — The Director shall ensure the National Drug Control Strategy is based on the best available evidence regarding the policies that are most effective in reducing the demand for and supply of illegal drugs.
(4) **Process for development and submission of National Drug Control Strategy** — In developing and effectively implementing the National Drug Control Strategy, the Director—
(A) shall consult with—
(i) the heads of the National Drug Control Program agencies;
(ii) each Coordinator listed in [section 1703 of this title](https:
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Source location: Title 21, Chapter 22, § 1705; chapter-022-national-drug-control-policy.md
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**(a) In general**
(1) **Statement of drug policy priorities** — The Director shall release a statement of drug control policy priorities in the calendar year of a Presidential inauguration following the inauguration, but not later than April 1.
(2) **National Drug Control Strategy submitted by the President** — Not later than the first Monday in February following the year in which the term of the President commences, and every 2 years thereafter, the President shall submit to Congress a National Drug Control Strategy.
**(b) Development of the National Drug Control Strategy**
(1) **Promulgation** — The Director shall promulgate the National Drug Control Strategy, which shall set forth a comprehensive plan to reduce illicit drug use and the consequences of such illicit drug use in the United States by limiting the availability of and reducing the demand for illegal drugs and promoting prevention, early intervention, treatment, and recovery support for individuals with substance use disorders.
(2) **State and local commitment** — The Director shall seek the support and commitment of State, local, and Tribal officials in the formulation and implementation of the National Drug Control Strategy.
(3) **Strategy based on evidence** — The Director shall ensure the National Drug Control Strategy is based on the best available evidence regarding the policies that are most effective in reducing the demand for and supply of illegal drugs.
(4) **Process for development and submission of National Drug Control Strategy** — In developing and effectively implementing the National Drug Control Strategy, the Director—
(A) shall consult with—
(i) the heads of the National Drug Control Program agencies;
(ii) each Coordinator listed in [section 1703 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1703&num=0&edition=prelim);
(iii) the Interdiction Committee and the Emerging Threats Committee;
(iv) the appropriate congressional committees and any other committee of jurisdiction;
(v) State, local, and Tribal officials;
(vi) private citizens and organizations, including community and faith-based organizations, with experience and expertise in demand reduction;
(vii) private citizens and organizations with experience and expertise in supply reduction; and
(viii) appropriate representatives of foreign governments; and
(B) in satisfying the requirements of subparagraph (A), shall ensure, to the maximum extent possible, that State, local, and Tribal officials and relevant private organizations commit to support and take steps to achieve the goals and objectives of the National Drug Control Strategy.
**(c) Contents of the National Drug Control Strategy**
(1) **In general** — The National Drug Control Strategy submitted under subsection (a)(2) shall include the following:
(A) A mission statement detailing the major functions of the National Drug Control Program.
(B) Comprehensive, research-based, long-range, quantifiable goals for reducing illicit drug use, and the consequences of illicit drug use in the United States.
(C) Annual quantifiable and measurable objectives and specific targets to accomplish long-term quantifiable goals that the Director determines may be achieved during each year beginning on the date on which the National Drug Control Strategy is submitted.
(D) A 5-year projection for the National Drug Control Program and budget priorities.
(E) A review of international, State, local, and private sector drug control activities to ensure that the United States pursues coordinated and effective drug control at all levels of government.
(F) A description of how each goal established under subparagraph (B) will be achieved, including for each goal—
(i) a list of each relevant National Drug Control Program agency and each such agency’s related programs, activities, and available assets and the role of each such program, activity, and asset in achieving such goal;
(ii) a list of relevant stakeholders and each such stakeholder’s role in achieving such goal;
(iii) an estimate of Federal funding and other resources needed to achieve such goal;
(iv) a list of each existing or new coordinating mechanism needed to achieve such goal; and
(v) a description of the Office’s role in facilitating the achievement of such goal.
(G) For each year covered by the Strategy, a performance evaluation plan for each goal established under subparagraph (B) for each National Drug Control Program agency, including—
(i) specific performance measures for each National Drug Control Program agency;
(ii) annual and, to the extent practicable, quarterly objectives and targets for each performance measure; and
(iii) an estimate of Federal funding and other resources needed to achieve each performance objective and target.
(H) A list identifying existing data sources or a description of data collection needed to evaluate performance, including a description of how the Director will obtain such data.
(I) A list of any anticipated challenges to achieving the National Drug Control Strategy goals and planned actions to address such challenges.
(J) A description of how each goal established under subparagraph (B) was determined, including—
(i) a description of each required consultation and a description of how such consultation was incorporated; and
(ii) data, research, or other information used to inform the determination to establish the goal.
(K) A description of the current prevalence of illicit drug use in the United States, including both the availability of illicit drugs and the prevalence of substance use disorders.
(L) Such other statistical data and information as the Director considers appropriate to demonstrate and assess trends relating to illicit drug use, the effects and consequences of illicit drug use (including the effects on children), supply reduction, demand reduction, drug-related law enforcement, and the implementation of the National Drug Control Strategy.
(M) A systematic plan for increasing data collection to enable real time surveillance of drug control threats, developing analysis and monitoring capabilities, and identifying and addressing policy questions related to the National Drug Control Strategy and Program, which shall include—
(i) a list of policy-relevant questions for which the Director and each National Drug Control Program agency intends to develop evidence to support the National Drug Control Program and Strategy;
(ii) a list of data the Director and each National Drug Control Program agency intends to collect, use, or acquire to facilitate the use of evidence in drug control policymaking and monitoring;
(iii) a list of methods and analytical approaches that may be used to develop evidence to support the National Drug Control Program and Strategy and related policy;
(iv) a list of any challenges to developing evidence to support policymaking, including any barriers to accessing, collecting, or using relevant data;
(v) a description of the steps the Director and the head of each National Drug Control Program agency will take to effectuate the plan; and
(vi) any other relevant information as determined by the Director.
(N) A plan to expand treatment of substance use disorders, which shall—
(i) identify unmet needs for treatment for substance use disorders and a strategy for closing the gap between available and needed treatment;
(ii) describe the specific roles and responsibilities of the relevant National Drug Control Program agencies for implementing the plan;
(iii) identify the specific resources required to enable the relevant National Drug Control Program agencies to implement that strategy; and
(iv) identify the resources, including private sources, required to eliminate the unmet need for evidence-based substance use disorder treatment.
(2) **Consultation** — In developing the plan required under paragraph (1)(M), the Director shall consult with the following:
(A) The public.
(B) Any evaluation or analysis units and personnel of the Office.
(C) Office officials responsible for implementing privacy policy.
(D) Office officials responsible for data governance.
(E) The appropriate congressional committees.
(F) Any other individual or entity as determined by the Director.
(3) **Additional strategies**
(A) *In general* — The Director shall include in the National Drug Control Strategy the additional strategies described under this paragraph and shall comply with the following:
(i) Provide a copy of the additional strategies to the appropriate congressional committees and to the Committee on Armed Services and the Committee on Homeland Security of the House of Representatives, and the Committee on Homeland Security and Governmental Affairs and the Committee on Armed Services of the Senate.
(ii) Issue the additional strategies in consultation with the head of each relevant National Drug Control Program agency, any relevant official of a State, local, or Tribal government, and the government of other relevant countries.
(iii) Not change any existing agency authority or construe any strategy described under this paragraph to amend or modify any law governing interagency relationship but may include recommendations about changes to such authority or law.
(iv) Present separately from the rest of any strategy described under this paragraph any information classified under criteria established by an Executive order, or whose public disclosure, as determined by the Director or the head of any relevant National Drug Control Program agency, would be detrimental to the law enforcement or national security activities of any Federal, State, local, or Tribal agency.
(B) *Requirement for Southwest Border Counternarcotics Strategy*
(i) *Purposes* — The Southwest Border Counternarcotics Strategy shall—
(I) set forth the Government’s strategy for preventing the illegal trafficking of drugs across the international border between the United States and Mexico, including through ports of entry and between ports of entry on that border;
(II) state the specific roles and responsibilities of the relevant National Drug Control Program agencies for implementing that strategy; and
(III) identify the specific resources required to enable the relevant National Drug Control Program agencies to implement that strategy.
(ii) *Specific content related to drug tunnels between the United States and Mexico* — The Southwest Border Counternarcotics Strategy shall include—
(I) a strategy to end the construction and use of tunnels and subterranean passages that cross the international border between the United States and Mexico for the purpose of illegal trafficking of drugs across such border; and
(II) recommendations for criminal penalties for persons who construct or use such a tunnel or subterranean passage for such a purpose.
(C) *Requirement for Northern Border Counternarcotics Strategy*
(i) *Purposes* — The Northern Border Counternarcotics Strategy shall—
(I) set forth the strategy of the Federal Government for preventing the illegal trafficking of drugs across the international border between the United States and Canada, including through ports of entry and between ports of entry on the border;
(II) state the specific roles and responsibilities of each relevant National Drug Control Program agency for implementing the strategy;
(III) identify the specific resources required to enable the relevant National Drug Control Program agencies to implement the strategy;
(IV) be designed to promote, and not hinder, legitimate trade and travel; and
(V) reflect the unique nature of small communities along the international border between the United States and Canada, ongoing cooperation and coordination with Canadian law,11 So in original. The comma probably should not appear. enforcement authorities, and variations in the volumes of vehicles and pedestrians crossing through ports of entry along the international border between the United States and Canada.
(ii) *Specific content related to cross-border Indian reservations* — The Northern Border Counternarcotics Strategy shall include—
(I) a strategy to end the illegal trafficking of drugs to or through Indian reservations on or near the international border between the United States and Canada; and
(II) recommendations for additional assistance, if any, needed by Tribal law enforcement agencies relating to the strategy, including an evaluation of Federal technical and financial assistance, infrastructure capacity building, and interoperability deficiencies.
(4) **Classified information** — Any contents of the National Drug Control Strategy that involve information properly classified under criteria established by an Executive order shall be presented to Congress separately from the rest of the National Drug Control Strategy.
(5) **Selection of data and information** — In selecting data and information for inclusion in the Strategy, the Director shall ensure—
(A) the inclusion of data and information that will permit analysis of current trends against previously compiled data and information where the Director believes such analysis enhances long-term assessment of the National Drug Control Strategy; and
(B) the inclusion of data and information to permit a standardized and uniform assessment of the effectiveness of drug treatment programs in the United States.
**(d) Submission of revised Strategy** The President may submit to Congress a revised National Drug Control Strategy that meets the requirements of this section—
(1) at any time, upon a determination of the President, in consultation with the Director, that the National Drug Control Strategy in effect is not sufficiently effective; or
(2) if a new President or Director takes office.
**(e) Failure of Director to Submit National Drug Control Strategy** If the Director does not submit a National Drug Control Strategy to Congress in accordance with subsection (a)(2), not later than five days after the first Monday in February following the year in which the term of the President commences, the Director shall send a notification to the appropriate congressional committees—
(1) explaining why the Strategy was not submitted; and
(2) specifying the date by which the Strategy will be submitted.
**(f) Drug Control Data Dashboard**
(1) **In general** — The Director shall collect and disseminate, as appropriate, such information as the Director determines is appropriate, but not less than the information described in this subsection. The data shall be publicly available in a machine-readable format on the online portal of the Office, and to the extent practicable on the Drug Control Data Dashboard.
(2) **Establishment** — The Director shall publish to the online portal of the Office in a machine-readable, sortable, and searchable format, or to the extent practicable, establish and maintain a data dashboard on the online portal of the Office to be known as the “Drug Control Data Dashboard”. To the extent practicable, when establishing the Drug Control Dashboard, the Director shall ensure the user interface of the dashboard is constructed with modern design standards. To the extent practicable, the data made available on the dashboard shall be publicly available in a machine-readable format and searchable by year, agency, drug, and location.
(3) **Data** — The data included in the Drug Control Data Dashboard shall be updated quarterly to the extent practicable, but not less frequently than annually and shall include, at a minimum, the following:
(A) For each substance identified by the Director as having a significant impact on the prevalence of illicit drug use—
(i) data sufficient to show the quantities of such substance available in the United States, including—
(I) the total amount seized and disrupted in the calendar year and each of the previous 3 calendar years, including to the extent practicable the amount seized by State, local, and Tribal governments;
(II) the known and estimated flows into the United States from all sources in the calendar year and each of the previous 3 calendar years;
(III) the total amount of known flows that could not be interdicted or disrupted in the calendar year and each of the previous 3 calendar years;
(IV) the known and estimated levels of domestic production in the calendar year and each of the previous three calendar years, including the levels of domestic production if the drug is a prescription drug, as determined under the Federal Food, Drug, and Cosmetic Act [[21 U.S.C. 301](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section301&num=0&edition=prelim) et seq.], for which a listing is in effect under [section 812 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section812&num=0&edition=prelim);
(V) the average street price for the calendar year and the highest known street price during the preceding 10-year period; and
(VI) to the extent practicable, related prosecutions by State, local, and Tribal governments; 22 So in original. Probably should be followed by “and”.
(ii) data sufficient to show the frequency of use of such substance, including—
(I) use of such substance in the workplace and productivity lost by such use;
(II) use of such substance by arrestees, probationers, and parolees;
(III) crime and criminal activity related to such substance; and
(IV) to the extent practicable, related prosecutions by State, local, and Tribal governments.
(B) For the calendar year and each of the previous three years data sufficient to show, disaggregated by State and, to the extent feasible, by region within a State, county, or city, the following:
(i) The number of fatal and non-fatal overdoses caused by each drug identified under subparagraph (A)(i).
(ii) The prevalence of substance use disorders.
(iii) The number of individuals who have received substance use disorder treatment, including medication assisted treatment, for a substance use disorder, including treatment provided through publicly-financed health care programs.
(iv) The extent of the unmet need for substance use disorder treatment, including the unmet need for medication-assisted treatment.
(C) Data sufficient to show the extent of prescription drug diversion, trafficking, and misuse in the calendar year and each of the previous 3 calendar years.
(D) Any quantifiable measures the Director determines to be appropriate to detail progress toward the achievement of the goals of the National Drug Control Strategy.
**(g) Development of an annual national drug control assessment**
(1) **Timing** — Not later than the first Monday in February of each year, the Director shall submit to the President, Congress, and the appropriate congressional committees, a report assessing the progress of each National Drug Control Program agency toward achieving each goal, objective, and target contained in the National Drug Control Strategy applicable to the prior fiscal year.
(2) **Process for development of the annual assessment** — Not later than November 1 of each year, the head of each National Drug Control Program agency shall submit, in accordance with guidance issued by the Director, to the Director an evaluation of progress by the agency with respect to the National Drug Control Strategy goals using the performance measures for the agency developed under this chapter, including progress with respect to—
(A) success in achieving the goals of the National Drug Control Strategy;
(B) success in reducing domestic and foreign sources of illegal drugs;
(C) success in expanding access to and increasing the effectiveness of substance use disorder treatment;
(D) success in protecting the borders of the United States (and in particular the Southwestern border of the United States) from penetration by illegal narcotics;
(E) success in reducing crime associated with drug use in the United States;
(F) success in reducing the negative health and social consequences of drug use in the United States;
(G) implementation of evidence-based substance use disorder treatment and prevention programs in the United States and improvements in the adequacy and effectiveness of such programs; and
(H) success in increasing the prevention of illicit drug use.
(3) **Contents of the annual assessment** — The Director shall include in the annual assessment required under paragraph (1)—
(A) a summary of each evaluation received by the Director under paragraph (2);
(B) a summary of the progress of each National Drug Control Program agency toward the National Drug Control Strategy goals of the agency using the performance measures for the agency developed under this chapter;
(C) an assessment of the effectiveness of each National Drug Control Program agency and program in achieving the National Drug Control Strategy for the previous year, including a specific evaluation of whether the applicable goals, measures, objectives, and targets for the previous year were met; and
(D) the assessments required under this subsection shall be based on the Performance Measurement System.33 So in original.
**(h) Performance measurement system** Not later than February 1 of each year, the Director shall submit to Congress as part of the National Drug Control Strategy, a description of a national drug control performance measurement system, that—
(1) develops 2-year and 5-year performance measures and targets for each National Drug Control Strategy goal and objective established for reducing drug use, availability, and the consequences of drug use;
(2) describes the sources of information and data that will be used for each performance measure incorporated into the performance measurement system;
(3) identifies major programs and activities of the National Drug Control Program agencies that support the goals and annual objectives of the National Drug Control Strategy;
(4) evaluates the contribution of demand reduction and supply reduction activities as defined in [section 1701 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1701&num=0&edition=prelim) implemented by each National Drug Control Program agency in support of the National Drug Control Strategy;
(5) monitors consistency between the drug-related goals and objectives of the National Drug Control Program agencies and ensures that each agency’s goals and budgets support and are fully consistent with the National Drug Control Strategy;
(6) coordinates the development and implementation of national drug control data collection and reporting systems to support policy formulation and performance measurement, including an assessment of—
(A) the quality of current drug use measurement instruments and techniques to measure supply reduction and demand reduction activities;
(B) the adequacy of the coverage of existing national drug use measurement instruments and techniques to measure the illicit drug user population, and groups that are at risk for illicit drug use;
(C) the adequacy of the coverage of existing national treatment outcome monitoring systems to measure the effectiveness of drug abuse treatment in reducing illicit drug use and criminal behavior during and after the completion of substance abuse treatment; and
(D) the actions the Director shall take to correct any deficiencies and limitations identified pursuant to subparagraphs (A) and (B) of this subsection; and
(7) develops performance measures and targets for the National Drug Control Strategy for supplemental strategies (the Southwest Border, Northern Border, and Caribbean Border Counternarcotics Strategies) to effectively evaluate region-specific goals, to the extent the performance measurement system does not adequately measure the effectiveness of the strategies, as determined by the Director, such strategies may evaluate interdiction efforts at and between ports of entry, interdiction technology, intelligence sharing, diplomacy, and other appropriate metrics, specific to each supplemental strategies region, as determined by the Director.
**(i) Modifications** A description of any modifications made during the preceding year to the national drug performance measurement system described in subsection (c) 44 Probably should be “(h)”. shall be included in each report submitted under subsection (b).55 Probably should be “(d)”.
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Federal law — U.S. Code and appendices · legal_authorities
This chapter may be cited as the Federal Food, Drug, and Cosmetic Act.
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Federal law — U.S. Code and appendices · legal_authorities
### Statutory Notes
Section, Pub. L. 105–277, div. C, title VII, § 715, Oct. 21, 1998, 112 Stat. 2681–693; Pub. L. 109–469, title VI, § 602, Dec. 29, 2006, 120 Stat. 3533; Pub. L. 115–271, title VIII, § 8202(a), Oct. 24, 2018, 132 Stat. 4110, provided for the termination of Office of National Drug Control Policy and repealed this chapter effective Sept. 30, 2010.
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Federal law — U.S. Code and appendices · legal_authorities
In this chapter:
(1) **Agency** — The term “agency” has the meaning given the term “executive agency” in [section 102 of title 31](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title31-section102&num=0&edition=prelim).
(2) **Appropriate congressional committees**
(A) *In general* — The term “appropriate congressional committees” means—
(i) the Committee on the Judiciary, the Committee on Appropriations, and the Committee on Health, Education, Labor, and Pensions of the Senate; and
(ii) the Committee on Oversight and Government Reform, the Committee on the Judiciary, the Committee on Energy and Commerce, and the Committee on Appropriations of the House of Representatives.
(B) *Submission to Congress* — Any submission to Congress shall mean submission to the appropriate congressional committees.
(3) **Demand reduction** — The term “demand reduction” means any activity conducted by a National Drug Control Program agency, other than an enforcement activity, that is intended to reduce or prevent the use of drugs or support, expand, or provide treatment and recovery efforts, including—
(A) education about the dangers of illicit drug use;
(B) services, programs, or strategies to prevent substance use disorder, including evidence-based education campaigns, community-based prevention programs, collection and disposal of unused prescription drugs, and services to at-risk populations to prevent or delay initial use of an illicit drug;
(C) substance use disorder treatment;
(D) support for long-term recovery from substance use disorders;
(E) drug-free workplace programs;
(F) drug testing, including the testing of employees;
(G) interventions for illicit drug use and dependence;
(H) expanding availability of access to health c
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Federal law — U.S. Code and appendices · legal_authorities
**(a) Appointment**
(1) **In general**
(A) *Director*
(i) *In general* — There shall be at the head of the Office a Director who shall hold the same rank and status as the head of an executive department listed in [section 101 of title 5](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title5-section101&num=0&edition=prelim).
(ii) *Appointment* — The Director shall be appointed by the President, by and with the advice and consent of the Senate, and shall serve at the pleasure of the President.
(B) *Deputy Director* — There shall be a Deputy Director who shall report directly to the Director, and who shall be appointed by the President, and shall serve at the pleasure of the President.
(C) *Coordinators* — The following coordinators shall be appointed by the Director:
(i) Performance Budget Coordinator, as described in subsection (c)(5).
(ii) Interdiction Coordinator, as described in [section 1710 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1710&num=0&edition=prelim).
(iii) Emerging and Continuing Threats Coordinator, as described in [section 1708 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1708&num=0&edition=prelim).
(iv) State, Local, and Tribal Affairs Coordinator, to carry out the activities described in subsection (j).
(v) Demand Reduction Coordinator, as described in subparagraph (D).
(D) *Demand Reduction Coordinator* — The Director shall designate or appoint a United States Demand Reduction Coordinator to be responsible for the activities described in [section 1701(3) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1701/3&num=0&edition=prelim). For purposes of carrying
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Federal law — U.S. Code and appendices · legal_authorities
**(a) Establishment** There are established five schedules of controlled substances, to be known as schedules I, II, III, IV, and V. Such schedules shall initially consist of the substances listed in this section. The schedules established by this section shall be updated and republished on a semiannual basis during the two-year period beginning one year after October 27, 1970, and shall be updated and republished on an annual basis thereafter.11 See Amendment of Schedules of Controlled Substances note below.
**(b) Placement on schedules; findings required** Except where control is required by United States obligations under an international treaty, convention, or protocol, in effect on October 27, 1970, and except in the case of an immediate precursor, a drug or other substance may not be placed in any schedule unless the findings required for such schedule are made with respect to such drug or other substance. The findings required for each of the schedules are as follows:
(1) **Schedule I.—**
(A) The drug or other substance has a high potential for abuse.
(B) The drug or other substance has no currently accepted medical use in treatment in the United States.
(C) There is a lack of accepted safety for use of the drug or other substance under medical supervision.
(2) **Schedule II.—**
(A) The drug or other substance has a high potential for abuse.
(B) The drug or other substance has a currently accepted medical use in treatment in the United States or a currently accepted medical use with severe restrictions.
(C) Abuse of the drug or other substances may lead to severe psychological or physical dependence.
(3) **Schedule III.—**
(A) The drug or other substance has a potential for abuse less than the drugs or other substances in schedules I and
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Federal law — U.S. Code and appendices · legal_authorities
**(a) Authority to make grants** As part of the program established under [section 1531 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1531&num=0&edition=prelim), the Director may award an initial grant under this subsection, and renewal grants under subsection (f), to any coalition awarded a grant under [section 1532 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1532&num=0&edition=prelim) that meets the criteria specified in subsection (d) in order to fund coalition mentoring activities by such coalition in support of the program.
**(b) Treatment with other grants**
(1) **Supplement** — A grant awarded to a coalition under this section is in addition to any grant awarded to the coalition under [section 1532 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1532&num=0&edition=prelim).
(2) **Requirement for basic grant** — A coalition may not be awarded a grant under this section for a fiscal year unless the coalition was awarded a grant or renewal grant under [section 1532(b) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1532/b&num=0&edition=prelim) for that fiscal year.
**(c) Application** A coalition seeking a grant under this section shall submit to the Administrator an application for the grant in such form and manner as the Administrator may require.
**(d) Criteria** A coalition meets the criteria specified in this subsection if the coalition—
(1) has been in existence for at least 5 years;
(2) has achieved, by or through its own efforts, measurable results in the prevention and treatment of substance use and misuse among youth;
(3) has staff or members willing to serve as mentors for
Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 1522
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Federal law — U.S. Code and appendices · legal_authorities
### Statutory Notes
Section 1503, Pub. L. 100–690, title I, § 1004, Nov. 18, 1988, 102 Stat. 4184, related to coordination between Office of National Drug Control Policy and executive branch departments and agencies. See [section 1704 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1704&num=0&edition=prelim).
Section 1504, Pub. L. 100–690, title I, § 1005, Nov. 18, 1988, 102 Stat. 4185; Pub. L. 103–322, title IX, § 90203, Sept. 13, 1994, 108 Stat. 1991; Pub. L. 105–20, § 2(b), June 27, 1997, 111 Stat. 234, related to annual development and submission of National Drug Control Strategy by President to Congress. See [section 1705 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1705&num=0&edition=prelim).
Section 1505, Pub. L. 100–690, title I, § 1008, formerly § 1003A, as added Pub. L. 101–510, div. A, title X, § 1011, Nov. 5, 1990, 104 Stat. 1633; renumbered § 1008 and amended Pub. L. 103–322, title IX, § 90204(a), (b), (c)(2), (3), Sept. 13, 1994, 108 Stat. 1993, 1994, established Counter-Drug Technology Assessment Center within Office of National Drug Control Policy.
A prior section 1505, Pub. L. 100–690, title I, § 1008, Nov. 18, 1988, 102 Stat. 4188, provided for an executive reorganization study and report to Congress and the President no later than Jan. 15, 1990, prior to repeal by Pub. L. 103–322, § 90204(c)(1).
#### Effective Date of Repeal
Repeal effective Sept. 30, 1997, see section 1009 of Pub. L. 100–690, as amended, which was formerly classified to [section 1506 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section1506&num=0&edition=prelim).
Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 1503 to 1505
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Federal law — U.S. Code and appendices · legal_authorities
**(a) United States Interdiction Coordinator**
(1) **In general** — The Director shall designate or appoint an appointee in the Senior Executive Service or an appointee in a position at level 15 of the General Schedule (or equivalent) as the United States Interdiction Coordinator to perform the duties of that position described in paragraph (2) and such other duties as may be determined by the Director with respect to coordination of efforts to interdict illicit drugs from entering the United States.
(2) **Responsibilities** — The United States Interdiction Coordinator shall be responsible to the Director for—
(A) coordinating the interdiction activities of the National Drug Control Program agencies to ensure consistency with the National Drug Control Strategy;
(B) on behalf of the Director, developing and issuing, on or before September 1 of each year and in accordance with paragraph (4), a National Interdiction Command and Control Plan to ensure the coordination and consistency described in subparagraph (A);
(C) assessing the sufficiency of assets committed to illicit drug interdiction by the relevant National Drug Control Program agencies; and
(D) advising the Director on the efforts of each National Drug Control Program agency to implement the National Interdiction Command and Control Plan.
(3) **Staff** — The Director shall assign such permanent staff of the Office as he considers appropriate to assist the United States Interdiction Coordinator to carry out the responsibilities described in paragraph (2), and may request that appropriate National Drug Control Program agencies detail or assign staff to assist in carrying out such responsibilities.
(4) **National Interdiction Command and Control Plan**
(A) *Purposes* — The National Interdiction Com
Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 1710
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Federal law — U.S. Code and appendices · legal_authorities
Page 973
TITLE 21—FOOD AND DRUGS
§ 1705
which was formerly classified principally to chapter 15
(§ 401 et seq.) of Title 50, War and National Defense,
prior to editorial reclassification in Title 50, and is now
classified principally to chapter 44 (§ 3001 et seq.) of
Title 50. For complete classification of this Act to the
Code, see Tables.
AMENDMENTS
2019—Pub. L. 116–74, § 2(a)(1), substituted ‘‘National
Drug Control Program agency’’ for ‘‘National Drug
Control Program Agency’’ wherever appearing.
Subsec. (d)(1). Pub. L. 116–74, § 2(a)(6)(A), substituted
‘‘than every’’ for ‘‘that every’’.
Subsec. (f)(1)(A)(i). Pub. L. 116–74, § 2(a)(6)(B)(i)(I),
substituted ‘‘grant; and’’ for ‘‘grant;’’.
Subsec. (f)(1)(C). Pub. L. 116–74, § 2(a)(6)(B)(i)(II), in-
serted ‘‘that may impede applicants’’ after ‘‘barriers’’
and struck out ‘‘impediments that applicants currently
have in the grant application process with applicable
agencies’’ before period at end.
Subsec. (f)(2). Pub. L. 116–74, § 2(a)(6)(B)(ii), sub-
stituted ‘‘Drug Control Program’’ for ‘‘Drug Control’’
in heading.
2018—Pub. L. 115–271, § 8202(b)(2), repealed Pub. L.
105–277, § 715. See 1998 Amendment note below.
Pub. L. 115–271, § 8202(a), revived and restored this sec-
tion as in effect on Sept. 29, 2003, and as amended by
Pub. L. 109–469 and Pub. L. 112–166. See Reauthorization
of the Office of National Drug Control Policy note set
out under section 1701 of this title.
Subsec. (d). Pub. L. 115–271, § 8217(g)(1), amended sub-
sec. (d) generally. Prior to amendment, text read as fol-
lows: ‘‘The Director shall—
‘‘(A) require the National Drug Control Program
agencies to submit to the Director not later than
February 1 of each year a detailed accounting of all
funds expended by the agencies for
Source: Supplied 2024 U.S. Code historical extraction · 21 U.S.C. § 1705
Stored review status: historical_2024_not_currentness_verified. Same stored citation; legal effect and authority still require review.
Federal law — U.S. Code and appendices · legal_authorities
Page 30
TITLE 21—FOOD AND DRUGS
§ 301
Sec.
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, terri-
torial, and tribal food safety officials.
399d.
Employee protections.
399e.
Nanotechnology.
399f.
Ensuring
adequate
information
regarding
pharmaceuticals for all populations, par-
ticularly underrepresented subpopulations,
including racial subgroups.
399g.
Food and Drug Administration Intercenter
Institutes.
399h.
National Centers of Excellence in Advanced
and Continuous Pharmaceutical Manufac-
turing.
399i.
Food and Drug Administration Working Cap-
ital Fund.
SUBCHAPTER I—SHORT TITLE
§ 301. Short title
This chapter may be cited as the Federal
Food, Drug, and Cosmetic Act.
(June 25, 1938, ch. 675, § 1, 52 Stat. 1040.)
Statutory Notes and Related Subsidiaries
EFFECTIVE DATE; POSTPONEMENT IN CERTAIN CASES
Act June 23, 1939, ch. 242, §§ 1, 2, 53 Stat. 853, 854, pro-
vided that:
‘‘[SEC. 1] (a) The effective date of the following provi-
sions of the Federal Food, Drug, and Cosmetic Act is
hereby postponed until January 1, 1940: Sections 402(c)
[342(c) of this title]; 403(e)(1) [343(e)(1) of this title];
403(g), (h), (i), (j), and (k) [343(g) to (k) of this title];
501(a), (4) [351(a)(4) of this title]; 502(b), (d), (e), (f), (g),
and (h) [352(b), (d) to (h) of this title]; 601(e) [361(e) of
this title]; and 602(b) [362(b) of this title].
‘‘(b) The Secretary of Agriculture shall promulgate
regulations further postponing to July 1, 1940[,] the ef-
fective date of the provisions of sections 403(e)(1)
[343(e)(1) of this title]; 403(g), (h), (i), (j), and (k) [343(g)
to (k)]; 502(b), (d), (
Source: Supplied 2024 U.S. Code historical extraction · 21 U.S.C. § 301
Stored review status: historical_2024_not_currentness_verified. The source passage cites 21 U.S.C. § 301. This identifies an authority to review, not proof of applicability.