Sec. 18-81q. Return of unused prescription drugs dispensed in correctional facilities to vendor pharmacies. Requirements. Regulations.
Sec. 18-81q. Return of unused prescription drugs dispensed in correctional
facilities to vendor pharmacies. Requirements. Regulations. (a) Each correctional
institution shall return to the vendor pharmacy which shall accept, for repackaging and
reimbursement to the Department of Correction, drug products that were dispensed to
a patient and not used if such drug products are (1) prescription drug products that are
not controlled substances, (2) sealed in individually packaged units, (3) returned to
the vendor pharmacy within the recommended period of shelf life for the purpose of
redispensing such drug products, (4) determined to be of acceptable integrity by a licensed pharmacist, and (5) oral and parenteral medication in single-dose sealed containers approved by the federal Food and Drug Administration, topical or inhalant drug
products in units of use containers approved by the federal Food and Drug Administration or parenteral medications in multiple-dose sealed containers approved by the federal
Food and Drug Administration from which no doses have been withdrawn.
(b) Notwithstanding the provisions of subsection (a) of this section:
(1) If such drug products are packaged in manufacturer's unit-dose packages, such
drug products shall be returned to the vendor pharmacy for redispensing and reimbursement to the Department of Correction if such drugs may be redispensed for use before
the expiration date, if any, indicated on the package.
(2) If such drug products are repackaged in manufacturer's unit-dose or multiple-dose blister packs, such drug products shall be returned to the vendor pharmacy for
redispensing and reimbursement to the Department of Correction if (A) the date on
which such drug product was repackaged, such drug product's lot number and expiration
date are indicated clearly on the package of such repackaged drug; (B) ninety days
or fewer have elapsed from the date of repackaging of such drug product; and (C) a
repackaging log is maintained by the pharmacy in the case of drug products repackaged
in advance of immediate needs.
(3) No drug products dispensed in a bulk dispensing container may be returned to
the vendor pharmacy.
(c) The Department of Correction shall establish procedures for the return of unused
drug products to the vendor pharmacy from which such drug products were purchased.
(d) The Department of Correction shall reimburse to the vendor pharmacy the reasonable cost of services incurred in the operation of this section, as determined by the
Commissioner of Correction.
(e) The Department of Consumer Protection, in consultation with the Department
of Correction, shall adopt regulations, in accordance with the provisions of chapter 54,
which shall govern the repackaging and labeling of drug products returned pursuant to
subsections (a) and (b) of this section. The Department of Consumer Protection shall
implement the policies and procedures necessary to carry out the provisions of this
section until January 1, 2003, while in the process of adopting such policies and procedures in regulation form, provided notice of intent to adopt the regulations is published
in the Connecticut Law Journal within twenty days after implementation.
(June Sp. Sess. P.A. 01-9, S. 27, 131; June 30 Sp. Sess. P.A. 03-6, S. 146(d); P.A. 04-169, S. 17; 04-189, S. 1.)
History: June Sp. Sess. P.A. 01-9 effective July 1, 2001; June 30 Sp. Sess. P.A. 03-6 and P.A. 04-169 replaced Department
of Consumer Protection with Department of Agriculture and Consumer Protection, effective July 1, 2004; P.A. 04-189
repealed Sec. 146 of June 30 Sp. Sess. P.A. 03-6, thereby reversing the merger of the Departments of Agriculture and
Consumer Protection, effective June 1, 2004.