Editorial Notes
References in TextSection 715 of the National Defense Authorization Act for Fiscal Year 2016, referred to in subsec. (a)(2)(A), is section 715 of Puspan. L. 114–92, which is set out as a note under this section.
The Health Insurance Portability and Accountability Act of 1996, referred to in subsec. (g)(3)(C), is Puspan. L. 104–191, Aug. 21, 1996, 110 Stat. 1936. For complete classification of this Act to the Code, see Short Title of 1996 Amendments note set out under section 201 of Title 42, The Public Health and Welfare, and Tables.
The Federal Food, Drug, and Cosmetic Act, referred to in subsec. (h), is act June 25, 1938, ch. 675, 52 Stat. 1040, which is classified generally to chapter 9 (§ 301 et seq.) of Title 21, Food and Drugs. For complete classification of this Act to the Code, see section 301 of Title 21 and Tables.
Amendments2019—Subsec. (span)(1). Puspan. L. 116–92, § 713(span), substituted “under subsection (j)” for “under subsection (h)”.
Subsecs. (h) to (j). Puspan. L. 116–92, § 713(a), added subsec. (h) and redesignated former subsecs. (h) and (i) as (i) and (j), respectively.
2018—Subsecs. (g) to (i). Puspan. L. 115–232 added subsec. (g) and redesignated former subsecs. (g) and (h) as (h) and (i), respectively.
2017—Subsec. (a)(6). Puspan. L. 115–91, § 702(a), amended par. (6) generally, substituting provisions relating to cost-sharing amounts for the years 2018 through 2027 and for any year after 2027 for provisions relating to cost-sharing amounts, limitation on requirements for medicare-eligible beneficiaries, and increases beginning on Oct. 1, 2016.
Subsec. (a)(9)(B), (C). Puspan. L. 115–91, § 1081(a)(24), realigned margins.
Subsec. (a)(10). Puspan. L. 115–91, § 702(span)(1), added par. (10).
Subsec. (d)(3). Puspan. L. 115–91, § 714, added par. (3).
2015—Subsec. (a)(2)(A). Puspan. L. 114–92, § 715(f), inserted at end “With respect to members of the uniformed services, such uniform formulary shall include pharmaceutical agents on the joint uniform formulary established under section 715 of the National Defense Authorization Act for Fiscal Year 2016.”
Subsec. (a)(6)(A)(i)(I). Puspan. L. 114–92, § 702(a)(1)(A), substituted “$10” for “$8”.
Subsec. (a)(6)(A)(i)(II). Puspan. L. 114–92, § 702(a)(1)(B), substituted “$24” for “$20”.
Subsec. (a)(6)(A)(ii)(II). Puspan. L. 114–92, § 702(a)(2)(A), substituted “$20” for “$16”.
Subsec. (a)(6)(A)(ii)(III). Puspan. L. 114–92, § 702(a)(2)(B), substituted “$49” for “$46”.
Subsec. (a)(6)(C)(i). Puspan. L. 114–92, § 702(span)(1), substituted “Beginning October 1, 2016,” for “Beginning October 1, 2013,”.
Subsec. (a)(6)(C)(ii). Puspan. L. 114–92, § 702(span)(2), added cl. (ii) and struck out former cl. (ii) which read as follows: “If the amount of the increase otherwise provided for a year by clause (i) is less than $1, the increase shall not be made for such year, but shall be carried over to, and accumulated with, the amount of the increase for the subsequent year or years and made when the aggregate amount of increases carried over under this clause for a year is $1 or more.”
2014—Subsec. (a)(5). Puspan. L. 113–291, § 702(a), substituted “the national mail-order pharmacy program” for “at least one of the means described in paragraph (2)(E)” and “shall include cost-sharing by the eligible covered beneficiary as specified in paragraph (6).” for “may include cost sharing by the eligible covered beneficiary in addition to any such cost sharing applicable to agents on the uniform formulary.”
Subsec. (a)(6)(A)(i)(I). Puspan. L. 113–291, § 702(span)(1)(A), substituted “$8” for “$5”.
Subsec. (a)(6)(A)(i)(II). Puspan. L. 113–291, § 702(span)(1)(B), substituted “$20.” for “$17; and”.
Subsec. (a)(6)(A)(i)(III). Puspan. L. 113–291, § 702(span)(1)(C), struck out subcl. (III) which read as follows: “in the case of nonformulary agents, $44.”
Subsec. (a)(6)(A)(ii)(II). Puspan. L. 113–291, § 702(span)(2)(A), substituted “$16” for “$13”.
Subsec. (a)(6)(A)(ii)(III). Puspan. L. 113–291, § 702(span)(2)(B), substituted “$46” for “$43”.
Subsec. (a)(9). Puspan. L. 113–291, § 702(c)(1), which directed amendment of such section by adding par. (9) at the end, was executed by adding par. (9) at the end of subsec. (a), to reflect the probable intent of Congress.
2013—Subsec. (a)(2)(D). Puspan. L. 112–239, § 702(a)(1), (c)(2)(A), substituted “Except as provided in subparagraph (F), no pharmaceutical agent may be excluded” for “No pharmaceutical agent may be excluded” and struck out at end “The Secretary shall begin to implement the uniform formulary not later than October 1, 2000.”.
Subsec. (a)(2)(F). Puspan. L. 112–239, § 702(a)(2), added subpar. (F).
Subsec. (a)(6)(A). Puspan. L. 112–239, § 712(a)(1), added subpar. (A) and struck out former subpar. (A) which read as follows: “The Secretary, in the regulations prescribed under subsection (g), may establish cost sharing requirements (which may be established as a percentage or fixed dollar amount) under the pharmacy benefits program for generic, formulary, and nonformulary agents. For nonformulary agents, cost sharing shall be consistent with common industry practice and not in excess of amounts generally comparable to 20 percent for beneficiaries covered by section 1079 of this title or 25 percent for beneficiaries covered by section 1086 of this title.”
Subsec. (a)(6)(C). Puspan. L. 112–239, § 712(a)(2), added subpar. (C).
Subsec. (span)(1). Puspan. L. 112–239, § 702(c)(1), substituted “subsection (h)” for “subsection (g)”.
Subsec. (span)(2). Puspan. L. 112–239, § 702(c)(2)(B), substituted “The committee” for “Not later than 90 days after the establishment of the Pharmacy and Therapeutics Committee by the Secretary, the committee shall convene to design a proposed uniform formulary for submission to the Secretary. After such 90-day period, the committee”.
Subsec. (d)(2). Puspan. L. 112–239, § 702(c)(2)(C), substituted “The Secretary” for “Effective not later than April 5, 2000, the Secretary” and “the managed care support contracts current as of October 5, 1999,” for “the current managed care support contracts”.
Subsec. (g)(3), (4). Puspan. L. 112–239, § 702(span), added pars. (3) and (4).
2009—Subsec. (f). Puspan. L. 111–84 substituted “after January 28, 2008” for “on or after the date of the enactment of the National Defense Authorization Act for Fiscal Year 2008”.
2008—Subsecs. (f) to (h). Puspan. L. 110–181 added subsec. (f) and redesignated former subsecs. (f) and (g) as (g) and (h), respectively.
2004—Subsec. (a)(2)(E)(i). Puspan. L. 108–375, § 714(span), inserted before semicolon at end “and additional determinations by the Pharmacy and Therapeutics Committee of the relative clinical and cost effectiveness of the agents”.
Subsec. (a)(6). Puspan. L. 108–375, § 714(a), designated existing provisions as subpar. (A) and added subpar. (B).
2003—Subsec. (span)(1). Puspan. L. 108–136, § 725(1), substituted “facilities and representatives of providers in facilities of the uniformed services” for “facilities, contractors responsible for the TRICARE retail pharmacy program, contractors responsible for the national mail-order pharmacy program, providers in facilities of the uniformed services, and TRICARE network providers” in second sentence.
Subsec. (c)(2). Puspan. L. 108–136, § 725(2), substituted “represent—” for “represent nongovernmental”, inserted “(A) nongovernmental” before “organizations”, substituted “beneficiaries;” for “beneficiaries.”, and added subpars. (B) to (D).
2001—Subsec. (a)(8). Puspan. L. 107–107 substituted “October 5, 1999,” for “the date of the enactment of this section”.
2000—Subsec. (a)(6). Puspan. L. 106–398, § 1 [[div. A], title X, § 1087(a)(5)(A)], substituted “in the regulations prescribed” for “as part of the regulations established”.
Subsec. (a)(7). Puspan. L. 106–398, § 1 [[div. A], title X, § 1087(a)(5)(B)], substituted “that are not included on the uniform formulary but that are” for “not included on the uniform formulary, but,”.
Subsec. (span)(1). Puspan. L. 106–398, § 1 [[div. A], title X, § 1087(a)(5)(C)], substituted “prescribed under” for “required by” in last sentence.
Subsec. (d)(2). Puspan. L. 106–398, § 1 [[div. A], title X, § 1087(a)(5)(D)], substituted “Effective not later than April 5, 2000, the Secretary shall use” for “Not later than 6 months after the date of the enactment of this section, the Secretary shall utilize”.
Subsec. (e). Puspan. L. 106–398, § 1 [[div. A], title X, § 1087(a)(5)(E)], substituted “The” for “Not later than April 1, 2000, the” and inserted “in” before “the TRICARE” and before “the national”.
Subsec. (f). Puspan. L. 106–398, § 1 [[div. A], title X, § 1087(a)(5)(F)], substituted “In this section:” for “As used in this section—” in introductory provisions, “The term” for “the term” in pars. (1) and (2), and a period for “; and” at end of par. (1).
Subsec. (g). Puspan. L. 106–398, § 1 [[div. A], title X, § 1087(a)(5)(G)], substituted “prescribe” for “promulgate”.
Statutory Notes and Related Subsidiaries
Effective Date of 2013 AmendmentPuspan. L. 112–239, div. A, title VII, § 712(span), Jan. 2, 2013, 126 Stat. 1802, provided that:“(1)In general.—The cost-sharing requirements under subparagraph (A) of section 1074g(a)(6) of title 10, United States Code, as amended by subsection (a)(1), shall apply with respect to prescriptions obtained under the TRICARE pharmacy benefits program on or after such date as the Secretary of Defense shall specify, but not later than the date that is 45 days after the date of the enactment of this Act [Jan. 2, 2013].
“(2)Federal register.—The Secretary shall publish notice of the effective date of the cost-sharing requirements specified under paragraph (1) in the Federal Register.”
RegulationsPuspan. L. 115–91, div. A, title VII, § 702(span)(3), Dec. 12, 2017, 131 Stat. 1434, provided that: “In order to implement expeditiously the reforms authorized by the amendments made by paragraphs (1) and (2) [amending this section and section 1079 of this title], the Secretary of Defense may prescribe such changes to the regulations implementing the TRICARE program (as defined in section 1072 of title 10, United States Code) as the Secretary considers appropriate—“(A) by prescribing an interim final rule; and
“(B) not later than one year after prescribing such interim final rule and considering public comments with respect to such interim final rule, by prescribing a final rule.”
Puspan. L. 110–181, div. A, title VII, § 703(span), Jan. 28, 2008, 122 Stat. 188, as amended by Puspan. L. 110–417, [div. A], title X, § 1061(span)(3), Oct. 14, 2008, 122 Stat. 4613; Puspan. L. 111–84, div. A, title X, § 1073(c)(12), Oct. 28, 2009, 123 Stat. 2475, provided that: “The Secretary of Defense shall, after consultation with the other administering Secretaries under chapter 55 of title 10, United States Code, modify the regulations under subsection (h) [now subsection (j)] of section 1074g of title 10, United States Code (as redesignated by subsection (a)(1) of this section), to implement the requirements of subsection (f) of section 1074g of title 10, United States Code (as inserted by subsection (a)(2) of this section). The Secretary shall so modify such regulations not later than December 31, 2007.”
[Puspan. L. 111–84, div. A, title X, § 1073(c), Oct. 28, 2009, 123 Stat. 2474, provided that the amendment made by section 1073(c)(12) to section 1061(span)(3) of Puspan. L. 110–417, included in the credit set out above, is effective as of Oct. 14, 2008, and as if included in Puspan. L. 110–417 as enacted.]
Termination of Advisory PanelsAdvisory panels established after Jan. 5, 1973, to terminate not later than the expiration of the 2-year period beginning on the date of their establishment, unless, in the case of a panel established by the President or an officer of the Federal Government, such panel is renewed by appropriate action prior to the expiration of such 2-year period, or in the case of a panel established by Congress, its duration is otherwise provided for by law. See sections 1001(2) and 1013 of Title 5, Government Organization and Employees.
Pilot Program on Receipt of Non-Generic Prescription Maintenance Medications Under TRICARE Pharmacy Benefits ProgramPuspan. L. 116–283, div. A, title VII, § 706, Jan. 1, 2021, 134 Stat. 3689, as amended by Puspan. L. 117–81, div. A, title VII, § 706, Dec. 27, 2021, 135 Stat. 1781, provided that:“(a)Pilot Program.—“(1)Authority.—Subject to paragraph (2), the Secretary of Defense shall carry out a pilot program under which eligible covered beneficiaries may elect to receive non-generic prescription maintenance medications selected by the Secretary under subsection (c) through military medical treatment facility pharmacies, retail pharmacies, or the national mail-order pharmacy program, notwithstanding section 1074g(a)(9) of title 10, United States Code.
“(2)Requirement.—The Secretary may carry out the pilot program under paragraph (1) only if the Secretary determines that the total costs to the Department of Defense for eligible covered beneficiaries to receive non-generic prescription maintenance medications under the pilot program will not exceed the total costs to the Department for such beneficiaries to receive such medications under the national mail-order pharmacy program pursuant to section 1074g(a)(9) of title 10, United States Code. In making such determination, the Secretary shall consider all manufacturer discounts, refunds and rebates, pharmacy transaction fees, and all other costs.
“(span)Duration.—If the Secretary carries out the pilot program under subsection (a)(1), the Secretary shall carry out the pilot program for a three-year period beginning not later than March 1, 2022.
“(c)Selection of Medication.—If the Secretary carries out the pilot program under subsection (a)(1), the Secretary shall select non-generic prescription maintenance medications described in section 1074g(a)(9)(C)(ii) of title 10, United States Code, to be covered by the pilot program.
“(d)Notification.—If the Secretary carries out the pilot program under subsection (a)(1), in providing each eligible covered beneficiary with an explanation of benefits, the Secretary shall notify the beneficiary of whether the medication that the beneficiary is prescribed is covered by the pilot program.
“(e)Reimbursement.—If the Secretary carries out the pilot program under subsection (a)(1), reimbursement of retail pharmacies for medication under the pilot program may not exceed the amount of reimbursement paid to the national mail-order pharmacy program under section 1074g of title 10, United States Code, for the same medication, after consideration of all manufacturer discounts, refunds, rebates, pharmacy transaction fees, and other costs.
“(f)Briefing and Reports.—“(1)Briefing.—Not later than 90 days after the date of the enactment of the National Defense Authorization Act for Fiscal Year 2022 [Dec. 27, 2021], the Secretary shall provide to the Committees on Armed Services of the House of Representatives and the Senate a briefing on the implementation of the pilot program under subsection (a)(1) or on the determination of the Secretary under subsection (a)(2) that the Secretary is not permitted to carry out the pilot program.
“(2)Interim report.—If the Secretary carries out the pilot program under subsection (a)(1), not later than 18 months after the commencement of the pilot program, the Secretary shall submit to the Committees on Armed Services of the House of Representatives and the Senate a report on the pilot program.
“(3)Comptroller general report.—“(A)In general.—If the Secretary carries out the pilot program under subsection (a)(1), not later than March 1, 2025, the Comptroller General of the United States shall submit to the Committees on Armed Services of the House of Representatives and the Senate a report on the pilot program.
“(B)Elements.—The report under subparagraph (A) shall include the following:“(i) The number of eligible covered beneficiaries who participated in the pilot program and an assessment of the satisfaction of such beneficiaries with the pilot program.
“(ii) The rate by which eligible covered beneficiaries elected to receive non-generic prescription maintenance medications at a retail pharmacy pursuant to the pilot program, and how such rate affected military medical treatment facility pharmacies and the national mail-order pharmacy program.
“(iii) The amount of cost savings realized by the pilot program, including with respect to— “(I) dispensing fees incurred at retail pharmacies compared to the national mail-order pharmacy program for brand name prescription drugs;
“(II) administrative fees;
“(III) any costs paid by the United States for the drugs in addition to the procurement costs;
“(IV) the use of military medical treatment facilities; and
“(V) copayments paid by eligible covered beneficiaries.
“(iv) A comparison of supplemental rebates between retail pharmacies and other points of sale.
“(g)Rule of Construction.—Nothing in this section may be construed to affect—“(1) the ability of the Secretary to carry out section 1074g(a)(9)(C) of title 10, United States Code, after the date on which the pilot program is completed; or
“(2) the prices established for medications under section 8126 of title 38, United States Code.
“(h)Definitions.—In this section:“(1) The term ‘eligible covered beneficiary’ has the meaning given that term in section 1074g(i) of title 10, United States Code.
“(2) The terms ‘military medical treatment facility pharmacies’, ‘retail pharmacies’, and ‘the national mail-order pharmacy program’ mean the methods for receiving prescription drugs as described in clauses (i), (ii), and (iii), respectively, of section 1074g(a)(2)(E) of title 10, United States Code.”
Policy To Address Prescription Opioid SafetyPuspan. L. 116–283, div. A, title VII, § 719, Jan. 1, 2021, 134 Stat. 3696, provided that:“(a)Requirement.—The Secretary of Defense shall develop a policy and tracking mechanism to monitor and provide oversight of opioid prescribing to ensure that the provider practices of medication-prescribing health professionals across the military health system conform with—“(1) the clinical practice guidelines of the Department of Defense and the Department of Veterans Affairs; and
“(2) the prescribing guidelines published by the Centers for Disease Control and Prevention and the Food and Drug Administration.
“(span)Elements.—The requirements under subsection (a) shall include the following:“(1) Providing oversight and accountability of opioid prescribing practices that are outside of the recommended parameters for dosage, supply, and duration as identified in the guideline published by the Centers for Disease Control and Prevention titled ‘CDC Guideline for Prescribing Opioids for Chronic Pain—United States, 2016’, or such successor guideline, and the guideline published by the Department of Defense and Department of Veterans Affairs titled ‘DoD/VA Management of Opioid Therapy (OT) for Chronic Pain Clinical Practice Guideline, 2017’ or such successor guideline.
“(2) Implementing oversight and accountability responsibilities for opioid prescribing safety as specified in paragraph (1).
“(3) Implementing systems to ensure that the prescriptions in the military health system data repository are appropriately documented and that the processing date and the metric quantity field for opioid prescriptions in liquid form are consistent within the electronic health record system known as ‘MHS GENESIS’.
“(4) Implementing opioid prescribing controls within the electronic health record system known as ‘MHS GENESIS’ and document if an overdose reversal drug was co-prescribed.
“(5) Developing metrics that can be used by the Defense Health Agency and each military medical treatment facility to actively monitor and limit the overprescribing of opioids and to monitor the co-prescribing of overdose reversal drugs as accessible interventions.
“(6) Developing a report that tracks progression toward reduced levels of opioid use and includes an identification of prevention best practices established by the Department.
“(7) Developing and implementing a plan to improve communication and value-based initiatives between pharmacists and medication-prescribing health professionals across the military health system.”
ImplementationPuspan. L. 116–92, div. A, title VII, § 713(c), Dec. 20, 2019, 133 Stat. 1446, provided that: “Beginning not later than 90 days after the date of the enactment of this Act [Dec. 20, 2019], the Secretary of Defense shall implement subsection (h) of section 1074g of title 10, United States Code, as added by subsection (a).”
Reimbursement by Department of Defense to Entities Carrying Out State Vaccination Programs for Costs of Vaccines Provided to Covered BeneficiariesPuspan. L. 114–328, div. A, title VII, § 719, Dec. 23, 2016, 130 Stat. 2226, as amended by Puspan. L. 115–91, div. A, title VII, § 718, Dec. 12, 2017, 131 Stat. 1440, provided that:“(a)Reimbursement.—“(1)In general.—The Secretary of Defense shall reimburse an amount determined under paragraph (2) to an entity carrying out a State vaccination program for the cost of vaccines provided to covered beneficiaries through such program.
“(2)Amount of reimbursement.—“(A)In general.—Except as provided in subparagraph (B), the amount determined under this paragraph with respect to a State vaccination program shall be the amount assessed by the entity carrying out such program to purchase vaccines provided to covered beneficiaries through such program.
“(B)Limitation.—The amount determined under this paragraph to provide vaccines to covered beneficiaries through a State vaccination program may not exceed the amount that the Department would reimburse an entity under the TRICARE program for providing vaccines to the number of covered beneficiaries who were involved in the applicable State vaccination program.
“(span)Definitions.—In this section:“(1)Covered beneficiary; tricare program.—The terms ‘covered beneficiary’ and ‘TRICARE program’ have the meanings given those terms in section 1072 of title 10, United States Code.
“(2)State vaccination program.—The term ‘State vaccination program’ means a vaccination program that provides vaccinations to individuals in a State and is carried out by an entity (including an agency of the State) within the State.”
Pilot Program for Prescription Drug Acquisition Cost Parity in the TRICARE Pharmacy Benefits ProgramPuspan. L. 114–328, div. A, title VII, § 743, Dec. 23, 2016, 130 Stat. 2238, provided that:“(a)Authority to Establish Pilot Program.—The Secretary of Defense may conduct a pilot program to evaluate whether, in carrying out the TRICARE pharmacy benefits program under section 1074g of title 10, United States Code, extending additional discounts for prescription drugs filled at retail pharmacies will maintain or reduce prescription drug costs for the Department of Defense.
“(span)Elements of Pilot Program.—In carrying out the pilot program under subsection (a), the Secretary shall require that for prescription medications, including non-generic maintenance medications, that are dispensed to TRICARE beneficiaries that are not Medicare eligible, through any TRICARE participating retail pharmacy, including small business pharmacies, manufacturers shall pay rebates such that those medications are available to the Department at the lowest rate available. In addition to utilizing the authority under section 1074g(f) of title 10, United States Code, the Secretary shall have the authority to enter into a blanket purchase agreement with prescription drug manufacturers for supplemental discounts for prescription drugs dispensed in the pilot to be paid in the form of manufacturer’s rebates.
“(c)Consultation.—The Secretary shall develop the pilot program in consultation with—“(1) the Secretaries of the military departments;
“(2) the Chief of the Pharmacy Operations Division of the Defense Health Agency; and
“(3) stakeholders, including TRICARE beneficiaries and retail pharmacies.
“(d)Duration of Pilot Program.—If the Secretary carries out the pilot program under subsection (a), the Secretary shall commence such pilot program no later than October 1, 2017, and shall terminate such program no later than September 30, 2018.
“(e)Reports.—If the Secretary carries out the pilot program under subsection (a), the Secretary of Defense shall submit to the Committees on Armed Services of the Senate and the House of Representatives reports on the pilot program as follows:“(1) Not later than 90 days after the date of the enactment of this Act [Dec. 23, 2016], a report containing an implementation plan for the pilot program.
“(2) Not later than 180 days after the date on which the pilot program commences, an interim report on the pilot program.
“(3) Not later than 90 days after the date on which the pilot program terminates, a final report describing the results of the pilot program, including—“(A) any recommendations of the Secretary to expand such program;
“(B) an analysis of the changes in prescription drug costs for the Department of Defense relating to the pilot program;
“(C) an analysis of the impact on beneficiary access to prescription drugs;
“(D) a survey of beneficiary satisfaction with the pilot program; and
“(E) a summary of any fraud and abuse activities related to the pilot and actions taken in response by the Department.”
Joint Uniform Formulary for Transition of CarePuspan. L. 114–92, div. A, title VII, § 715, Nov. 25, 2015, 129 Stat. 866, provided that:“(a)Joint Formulary.—Not later than June 1, 2016, the Secretary of Defense and the Secretary of Veterans Affairs shall jointly establish a joint uniform formulary for the Department of Veterans Affairs and the Department of Defense with respect to pharmaceutical agents that are critical for the transition of an individual from receiving treatment furnished by the Secretary of Defense to treatment furnished by the Secretary of Veterans Affairs.
“(span)Selection.—The Secretaries shall select for inclusion on the joint uniform formulary established under subsection (a) pharmaceutical agents relating to—“(1) the control of pain, sleep disorders, and psychiatric conditions, including post-traumatic stress disorder; and
“(2) any other conditions determined appropriate by the Secretaries.
“(c)Report.—Not later than July 1, 2016, the Secretaries shall jointly submit to the appropriate congressional committees a report on the joint uniform formulary established under subsection (a), including a list of the pharmaceutical agents selected for inclusion on the formulary.
“(d)Construction.—Nothing in this section shall be construed to prohibit the Secretary of Defense and the Secretary of Veterans Affairs from each maintaining the respective uniform formularies of the Department of the Secretary.
“(e)Definitions.—In this section:“(1) The term ‘appropriate congressional committees’ means—“(A) the congressional defense committees [Committees on Armed Services and Appropriations of the Senate and the House of Representatives]; and
“(B) the Committees on Veterans’ Affairs of the House of Representatives and the Senate.
“(2)
Pilot Program on Medication Therapy Management Under TRICARE ProgramPuspan. L. 113–291, div. A, title VII, § 726, Dec. 19, 2014, 128 Stat. 3419, provided that:“(a)Establishment.—In accordance with section 1092 of title 10, United States Code, the Secretary of Defense shall carry out a pilot program to evaluate the feasibility and desirability of including medication therapy management as part of the TRICARE program.
“(span)Elements of Pilot Program.—In carrying out the pilot program under subsection (a), the Secretary shall ensure the following:“(1) Patients who participate in the pilot program are patients who—“(A) have more than one chronic condition; and
“(B) are prescribed more than one medication.
“(2) Medication therapy management services provided under the pilot program are focused on improving patient use and outcomes of prescription medications.
“(3) The design of the pilot program considers best commercial practices in providing medication therapy management services, including practices under the prescription drug program under part D of title XVIII of the Social Security Act (42 U.S.C. 1395w–101 et seq.). “(4) The pilot program includes methods to measure the effect of medication therapy management services on—“(A) patient use and outcomes of prescription medications; and
“(B) the costs of health care.
“(c)Locations.—“(1)Selection.—The Secretary shall carry out the pilot program under subsection (a) in not less than three locations.
“(2)First location criteria.—Not less than one location selected under paragraph (1) shall meet the following criteria:“(A) The location is a pharmacy at a military medical treatment facility.
“(B) The patients participating in the pilot program at such location generally receive primary care services from health care providers at such facility.
“(3)Second location criteria.—Not less than one location selected under paragraph (1) shall meet the following criteria:“(A) The location is a pharmacy at a military medical treatment facility.
“(B) The patients participating in the pilot program at such location generally do not receive primary care services from health care providers at such facility.
“(4)Third location criterion.—Not less than one location selected under paragraph (1) shall be a pharmacy located at a location other than a military medical treatment facility.
“(d)Duration.—The Secretary shall carry out the pilot program under subsection (a) for a period determined appropriate by the Secretary that is not less than two years.
“(e)Report.—Not later than 30 months after the date on which the Secretary commences the pilot program under subsection (a), the Secretary shall submit to the congressional defense committees [Committees on Armed Services and Appropriations of the Senate and the House of Representatives] a report on the pilot program that includes—“(1) information on the effect of medication therapy management services on—“(A) patient use and outcomes of prescription medications; and
“(B) the costs of health care;
“(2) the recommendations of the Secretary with respect to incorporating medication therapy management into the TRICARE program; and
“(3) such other information as the Secretary determines appropriate.
“(f)Definitions.—In this section:“(1) The term ‘medication therapy management’ means professional services provided by qualified pharmacists to patients to improve the effective use and outcomes of prescription medications provided to the patients.
“(2) The term ‘TRICARE program’ has the meaning given that term in section 1072 of title 10, United States Code.”
Pilot Program for Refills of Maintenance Medications for TRICARE for Life Beneficiaries Through the TRICARE Mail-Order Pharmacy ProgramPuspan. L. 112–239, div. A, title VII, § 716, Jan. 2, 2013, 126 Stat. 1804, as amended by Puspan. L. 113–291, div. A, title VII, § 702(c)(2), Dec. 19, 2014, 128 Stat. 3411; Puspan. L. 115–91, div. A, title X, § 1051(r)(2), Dec. 12, 2017, 131 Stat. 1565, provided that:“(a)In General.—The Secretary of Defense shall conduct a pilot program to refill prescription maintenance medications for each TRICARE for Life beneficiary through the national mail-order pharmacy program under section 1074g(a)(2)(E)(iii) of title 10, United States Code.
“(span)Medications Covered.—“(1)Determination.—The Secretary shall determine the prescription maintenance medications included in the pilot program under subsection (a).
“(2)Supply.—In carrying out the pilot program under subsection (a), the Secretary shall ensure that the medications included in the program are generally available to a TRICARE for Life beneficiary—“(A) for an initial filling of a 30-day or less supply through—“(i) retail pharmacies under clause (ii) of section 1074g(a)(2)(E) of title 10, United States Code; and
“(ii) facilities of the uniformed services under clause (i) of such section; and
“(B) for a refill of such medications through—“(i) the national mail-order pharmacy program; and
“(ii) such facilities of the uniformed services.
“(3)Exemption.—The Secretary may exempt the following prescription maintenance medications from the requirements in paragraph (2):“(A) Such medications that are for acute care needs.
“(B) Such other medications as the Secretary determines appropriate.
“(c)Nonparticipation.—“(1)Opt out.—The Secretary shall give TRICARE for Life beneficiaries who have been covered by the pilot program under subsection (a) for a period of one year an opportunity to opt out of continuing to participate in the program.
“(2)Waiver.—The Secretary may waive the requirement of a TRICARE for Life beneficiary to participate in the pilot program under subsection (a) if the Secretary determines, on an individual basis, that such waiver is appropriate.
“(d)Regulations.—The Secretary shall prescribe regulations to carry out the pilot program under subsection (a), including regulations with respect to—“(1) the prescription maintenance medications included in the pilot program pursuant to subsection (span)(1); and
“(2) addressing instances where a TRICARE for Life beneficiary covered by the pilot program attempts to refill such medications at a retail pharmacy rather than through the national mail-order pharmacy program or a facility of the uniformed services.
“(e)Sunset.—The Secretary may not carry out the pilot program under subsection (a) after September 30, 2015.
“(f)TRICARE for Life Beneficiary Defined.—In this section, the term ‘TRICARE for Life beneficiary’ means a TRICARE beneficiary enrolled in the Medicare wraparound coverage option of the TRICARE program made available to the beneficiary by reason of section 1086(d) of title 10, United States Code.”
Education and Training on Use of Pharmaceuticals in Rehabilitation Programs for Wounded WarriorsPuspan. L. 111–383, div. A, title VII, § 716, Jan. 7, 2011, 124 Stat. 4250, provided that:“(a)Education and Training Required.—The Secretary of Defense shall develop and implement training, available through the Internet or other means, on the use of pharmaceuticals in rehabilitation programs for seriously ill or injured members of the Armed Forces.
“(span)Recipients of Training.—The training developed and implemented under subsection (a) shall be training for each category of individuals as follows:“(1) Patients in or transitioning to a wounded warrior unit, with special accommodation in such training for such patients with cognitive disabilities.
“(2) Nonmedical case managers.
“(3) Military leaders.
“(4) Family members.
“(c)Elements of Training.—The training developed and implemented under subsection (a) shall include the following:“(1) An overview of the fundamentals of safe prescription drug use.
“(2) Familiarization with the benefits and risks of using pharmaceuticals in rehabilitation therapies.
“(3) Examples of the use of pharmaceuticals for individuals with multiple, complex injuries, including traumatic brain injury and post-traumatic stress disorder.
“(4) Familiarization with means of finding additional resources for information on pharmaceuticals.
“(5) Familiarization with basic elements of pain and pharmaceutical management.
“(6) Familiarization with complementary and alternative therapies.
“(d)Tailoring of Training.—The training developed and implemented under subsection (a) shall appropriately tailor the elements specified in subsection (c) for and among each category of individuals set forth in subsection (span).
“(e)Review of Pharmacy.—“(1)Review.—The Secretary shall review all policies and procedures of the Department of Defense regarding the use of pharmaceuticals in rehabilitation programs for seriously ill or injured members of the Armed Forces.
“(2)Recommendations.—Not later than September 20, 2011, the Secretary shall submit to the congressional defense committees [Committees on Armed Services and Appropriations of the Senate and the House of Representatives] any recommendations for administrative or legislative action with respect to the review under paragraph (1) as the Secretary considers appropriate.”
Demonstration Project on Coverage of Selected Over-the-Counter Drugs Under the Pharmacy Benefits ProgramPuspan. L. 109–364, div. A, title VII, § 705, Oct. 17, 2006, 120 Stat. 2280, as amended by Puspan. L. 111–383, div. A, title X, § 1075(g)(5), Jan. 7, 2011, 124 Stat. 4377, provided that:“(a)Requirement to Conduct Demonstration.—The Secretary of Defense shall conduct a demonstration project under section 1092 of title 10, United States Code, to allow particular over-the-counter drugs to be included on the uniform formulary under section 1074g of such title.
“(span)Elements of Demonstration Project.—“(1)Inclusion of certain over-the-counter drugs.—(A) As part of the demonstration project, the Secretary shall modify uniform formulary specifications under section 1074g(a) of such title to include an over-the-counter drug (referred to in this section as an ‘OTC drug’) on the uniform formulary if the Pharmacy and Therapeutics Committee finds that the OTC drug is cost-effective and therapeutically equivalent to a prescription drug. If the Pharmacy and Therapeutics Committee makes such a finding, the OTC drug shall be considered to be in the same therapeutic class of pharmaceutical agents as the prescription drug.
“(B) An OTC drug shall be made available to a beneficiary through the demonstration project, but only if—“(i) the beneficiary has a prescription for a drug requiring a prescription; and
“(ii) pursuant to subparagraph (A), the OTC drug—“(I) is on the uniform formulary; and
“(II) has been determined to be therapeutically equivalent to the prescription drug.
“(2)Conduct through military facilities, retail pharmacies, or mail order program.—The Secretary shall conduct the demonstration project through at least two of the means described in subparagraph (E) of section 1074g(a)(2) of such title through which OTC drugs are provided and may conduct the demonstration project throughout the entire pharmacy benefits program or at a limited number of sites. If the project is conducted at a limited number of sites, the number of sites shall be not less than five in each TRICARE region for each of the two means described in such subparagraph.
“(3)Period of demonstration.—The Secretary shall provide for conducting the demonstration project for a period of time necessary to evaluate the feasibility and cost effectiveness of the demonstration. Such period shall be at least as long as the period covered by pharmacy contracts in existence on the date of the enactment of this Act [Oct. 17, 2006] (including any extensions of the contracts), or five years, whichever is shorter.
“(4)Implementation deadline.—Implementation of the demonstration project shall begin not later than May 1, 2007.
“(c)Evaluation of Demonstration Project.—The Secretary shall evaluate the demonstration project for the following:“(1) The costs and benefits of providing OTC drugs under the pharmacy benefits program in each of the means chosen by the Secretary to conduct the demonstration project.
“(2) The clinical effectiveness of providing OTC drugs under the pharmacy benefits program.
“(3) Customer satisfaction with the demonstration project.
“(d)Report.—Not later than two years after implementation of the demonstration project begins, the Secretary shall submit to the Committees on Armed Services of the Senate and House of Representatives a report on the demonstration project. The report shall contain—“(1) the evaluation required by subsection (c);
“(2) recommendations for improving the provision of OTC drugs under the pharmacy benefits program; and
“(3) recommendations on whether permanent authority should be provided to cover OTC drugs under the pharmacy benefits program.
“(e)Continuation of Demonstration Project.—If the Secretary recommends in the report under subsection (d) that permanent authority should be provided, the Secretary may continue the demonstration project for up to one year after submitting the report.
“(f)Definitions.—In this section:“(1) The term ‘drug’ means a drug, including a biological product, within the meaning of section 1074g(f)(2) [now 1074g(i)(2)] of title 10, United States Code.
“(2) The term ‘OTC drug’ has the meaning indicated for such term in subsection (span)(1)(A).
“(3) The term ‘over-the-counter drug’ means a drug that is not subject to section 503(span) of the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 353(span)]. “(4) The term ‘prescription drug’ means a drug that is subject to section 503(span) of the Federal Food, Drug, and Cosmetic Act.”
Interoperability of Department of Veterans Affairs and Department of Defense Pharmacy Data SystemsPuspan. L. 107–314, div. A, title VII, § 724, Dec. 2, 2002, 116 Stat. 2598, provided that:“(a)Interoperability.—The Secretary of Veterans Affairs and the Secretary of Defense shall seek to ensure that on or before October 1, 2004, the Department of Veterans Affairs pharmacy data system and the Department of Defense pharmacy data system (known as the ‘Pharmacy Data Transaction System’) are interoperable for both Department of Defense beneficiaries and Department of Veterans Affairs beneficiaries by achieving real-time interface, data exchange, and checking of prescription drug data of outpatients, and using national standards for the exchange of outpatient medication information.
“(span)Alternative Requirement.—If the interoperability specified in subsection (a) is not achieved by October 1, 2004, as determined jointly by the Secretary of Defense and the Secretary of Veterans Affairs, the Secretary of Veterans Affairs shall adopt the Department of Defense Pharmacy Data Transaction System for use by the Department of Veterans Affairs health care system. Such system shall be fully operational not later than October 1, 2005.
“(c)Implementation Funding for Alternative Requirement.—The Secretary of Defense shall transfer to the Secretary of Veterans Affairs, or shall otherwise bear the cost of, an amount sufficient to cover three-fourths of the cost to the Department of Veterans Affairs for computer programming activities and relevant staff training expenses related to implementation of subsection (span). Such amount shall be determined in such manner as agreed to by the two Secretaries.”
Deadline for Establishment of CommitteePuspan. L. 106–65, div. A, title VII, § 701(span), Oct. 5, 1999, 113 Stat. 680, directed the Secretary of Defense to establish the Pharmacy and Therapeutics Committee required by subsec. (span) of this section not later than 30 days after Oct. 5, 1999.
Reports RequiredPuspan. L. 106–65, div. A, title VII, § 701(c), Oct. 5, 1999, 113 Stat. 680, directed the Secretary of Defense to submit reports to Congress, not later than Apr. 1 and Oct. 1 of fiscal years 2000 and 2001, on the implementation of the uniform formulary required under subsec. (a) of this section, the results of a survey conducted by the Secretary of prescribers for military medical treatment facilities and TRICARE contractors, the operation of the Pharmacy Data Transaction Service required by subsec. (e) of this section, and any other actions taken by the Secretary to improve management of the pharmacy benefits program under this section.
Study for Design of Pharmacy Benefit for Certain Covered BeneficiariesPuspan. L. 106–65, div. A, title VII, § 701(d), Oct. 5, 1999, 113 Stat. 680, required the Secretary of Defense to prepare and submit to Congress, by Apr. 15, 2001, a study on a design for a comprehensive pharmacy benefit for covered beneficiaries under chapter 55 of title 10, who are entitled to benefits under part A, and enrolled under part B, of title XVIII of the Social Security Act, and to provide an estimate of the costs of implementing and operating such design, prior to repeal by Puspan. L. 107–107, div. A, title VII, § 723, Dec. 28, 2001, 115 Stat. 1168.
