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20-77-1403. Definitions.
Arkansas Code — all titles (historical 2020) · legal_authorities
20-77-1403. Definitions.
As used in this subchapter:
(1) [Repealed.]
(2) “Medicaid” means the Arkansas program of medical assistance established under Title XIX of the Social Security Act;
(3) “Prescription Drug Access Program” means the limited prescription drug benefit Medicaid waiver program established under this subchapter;
(4) “Prescription drugs” means controlled substances and legend drugs as defined in § 20-64-503; and
(5) “Waiver” means the limited prescription drug benefit Medicaid waiver authorized by this subchapter.
Source: Arkansas Code — historical release 78 (November 6, 2020) · 20-77-1403
Stored review status: Historical 2020-11-06 source release; later amendments not reconciled; machine-extracted, not independently legally reviewed; source heading status: text_in_historical_source. A text match is a research starting point; applicability is not established.
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Record provenance
Stable record: arkansas_code:legal_authorities:20-77-1403
Source file: gov.ar.code.title.20.odt
Pages: Not recorded – Not recorded
Passage SHA-256: e63031ded9c6863a80a0b7bdc6ae4877b78113929ec74dbac7b2b79a88d255fb
Source location: content.xml paragraph 37148
Stored source content
20-77-1403. Definitions.
As used in this subchapter:
(1) [Repealed.]
(2) “Medicaid” means the Arkansas program of medical assistance established under Title XIX of the Social Security Act;
(3) “Prescription Drug Access Program” means the limited prescription drug benefit Medicaid waiver program established under this subchapter;
(4) “Prescription drugs” means controlled substances and legend drugs as defined in § 20-64-503; and
(5) “Waiver” means the limited prescription drug benefit Medicaid waiver authorized by this subchapter.
Cross-references
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Arkansas Code — all titles (historical 2020) · legal_authorities
20-64-503. Definitions.
As used in this subchapter, unless the context otherwise requires:
(1) “Blood” means whole blood collected from a single donor and processed either for transfusion or further manufacturing;
(2) “Blood component” means that part of blood separated by physical or mechanical means;
(3) [Repealed.]
(4) “Controlled substance” means those substances, drugs, or immediate precursors listed in Schedules I through VI of the Uniform Controlled Substances Act, § 5-64-101 et seq., and revised by the Secretary of the Department of Health pursuant to his or her authority under §§ 5-64-214 — 5-64-216;
(5) “Drug sample” means a unit of a prescription drug that is not intended to be sold and is intended to promote the sale of the drug;
(6)(A) “Legend drug” means a drug limited by section 503(b)(1) of the Federal Food, Drug, and Cosmetic Act to being dispensed by or upon a medical practitioner's prescription because the drug is:
(i) Habit-forming;
(ii) Toxic or having potential for harm; or
(iii) Limited in its use to use under a practitioner's supervision by the new drug application for the drug.
(B) The product label of a legend drug is required to contain the statement: “CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION”.
(C) A legend drug includes prescription drugs subject to the requirement of section 503(b)(1) of the Federal Food, Drug, and Cosmetic Act which shall be exempt from section 502(f)(1) if certain specified conditions are met;
(7) “Manufacturer” means anyone who is engaged in manufacturing, preparing, propagating, compounding, processing, packaging, repackaging, or labeling of a prescription drug;
(8) “Person” includes individual, partnership, corporation, business firm, and association;
(9) “Prescriptio
Source: Arkansas Code — historical release 78 (November 6, 2020) · 20-64-503
Stored review status: Historical 2020-11-06 source release; later amendments not reconciled; machine-extracted, not independently legally reviewed; source heading status: text_in_historical_source. The source passage cites 20-64-503. This identifies an authority to review, not proof of applicability.