Ariz. Admin. Code § R4-16-303 - Prescribing and Dispensing Requirements
A. A physician shall record on the patient's
medical record the name, strength, dosage, and form, of a controlled substance,
prescription-only drug, or prescription-only device dispensed, the quantity or
volume dispensed, the date the controlled substance, prescription-only drug, or
prescription-only device is dispensed, the therapeutic reason for dispensing
the controlled substance, prescription-only drug, or prescription-only device,
and the number of refills authorized.
B. Before dispensing a controlled substance,
prescription-only drug, or prescription-only device to a patient, a physician
shall review the prepared controlled substance, prescription-only drug, or
prescription-only device to ensure:
1. The
container label and contents comply with the prescription order, and
2. The patient is informed of the name of the
controlled substance, prescription-only drug, or prescription-only device,
directions for use, precautions, and storage requirements.
C. A physician shall purchase all dispensed
controlled substances, prescription-only drugs, or prescription-only devices
from a manufacturer or distributor approved by the United States Food and Drug
Administration or a pharmacy holding a current permit from the Arizona Board of
Pharmacy.
D. The person who
prepares a controlled substance, prescription-only drug, or prescription-only
device for dispensing shall countersign and date the original prescription
order for the controlled substance, prescription-only drug, or
prescription-only device.
E. For purposes of this Article, "dispensing" means the
delivery of a controlled substance, a prescription-only drug, or a
prescription-only device to a patient for use outside the physician's
office.
Notes
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