Oklahoma Code § 63-1-1918.1

Title 63. Public Health And Safety: Dispensation of certain drugs in bubble pack units -
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Pilot program.
A.  The purpose of this section is to reduce expensive and
unnecessary wastage of excess drugs dispensed to residents of
nursing homes.  In order to determine if the use of bubble pack
units and the return and reissuance of unadulterated drugs is cost-
effective and administratively efficient there is hereby established
a pilot program for dispensing and returning anti-ulcer and
antiarthritics in bubble pack units.  The pilot program shall
terminate January 1, 1998.
B.  For the purpose of this study, upon filling a prescription
for residents of nursing facilities, a pharmacist shall dispense
anti-ulcer and antiarthritics in bubble pack units when available.
C.  Any prescription for anti-ulcer and antiarthritics dispensed
by a pharmacist in bubble pack units for a resident of a nursing
home that is unused and is unadulterated may be returned for credit
to the issuing pharmacy.  Such medication may be dispensed by the

pharmacist to other nursing home patients.  The Oklahoma Health Care
Authority in concert with the State Board of Pharmacy shall
promulgate permanent rules that will provide for the implementation
of this subsection.  The permanent rules shall be promulgated by the
Board pursuant to the provisions of the Administrative Procedures
Act.
D.  The Oklahoma State Board of Health in concert with the State
Board of Pharmacy shall promulgate rules to ensure the integrity of
the collection of unadulterated anti-ulcer and antiarthritics within
nursing facilities.  The rules shall provide for a drug manifest
form that shall accompany each shipment of unadulterated anti-ulcer
and antiarthritics in bubble pack units from the nursing facility to
the dispensing pharmacy.
E.  The State Board of Health shall report the findings of the
pilot program to the Speaker of the House of Representatives, the
President Pro Tempore of the Senate and the Governor by April 1,
1998.
F.  For purposes of this section:
1.  "Bubble pack units" means a sealed unit of use container
packaged by a pharmacy or pharmaceutical manufacturer that bears the
name of the drug, expiration date, and the name of the pharmacy
dispensing the drug;
2.  "Nursing facility" means a facility as defined by Section 1-
1902 of Title 63 of the Oklahoma Statutes;
3.  "Unadulterated" means medications that are properly stored,
labeled and not past the expiration date; and
4.  "Antiarthritics" means legend nonsteroidal anti-inflammatory
drugs.

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