Connecticut § 17b-499 Pharmacy outreach program: Definitions.

Connecticut Statutes

§ 17b-499 — Pharmacy outreach program: Definitions.

Connecticut § 17b-499

Title 17bSocial Services

Ch. 319ffPrescription Drug Assistance

This text of Connecticut § 17b-499 (Pharmacy outreach program: Definitions.) is published on Counsel Stack Legal Research, covering Connecticut primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

Conn. Gen. Stat. § 17b-499 (2026).

Text

As used in this section and section 17b-499a:

(1)“Eligible person” means any person who is a resident of Connecticut at the time such person files an application for prescription medications or nonprescription medications with a participating manufacturer;

(2)“Department” means the Department of Social Services;

(3)“Participating manufacturer” means a pharmaceutical manufacturer that offers prescription medications or nonprescription medications at a reduced cost or at no cost to persons pursuant to a voluntary drug assistance program established by such manufacturer;

(4)“Prescription medications” means prescription drugs that have been approved as safe and effective by the federal Food and Drug Administration or that are otherwise legally marketed and manufactured in the United States

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As used in this section and section 17b-499a: (1) “Eligible person” means any person who is a resident of Connecticut at the time such person files an application for prescription medications or nonprescription medications with a participating manufacturer; (2) “Department” means the Department of Social Services; (3) “Participating manufacturer” means a pharmaceutical manufacturer that offers prescription medications or nonprescription medications at a reduced cost or at no cost to persons pursuant to a voluntary drug assistance program established by such manufacturer; (4) “Prescription medications” means prescription drugs that have been approved as safe and effective by the federal Food and Drug Administration or that are otherwise legally marketed and manufactured in the United States and manufactured and offered by pharmaceutical companies.