Or. Admin. Code § 855-041-1130 - Retail Drug Outlet Pharmacy Prescription Labeling
Except as described in SB 450 (2023), prescriptions must be labeled with the following information:
(1) Name, address and telephone number of the
pharmacy;
(2) Date of
fill;
(3) Identifying
number;
(4) Name of
patient;
(5) Name of drug,
strength, and quantity dispensed; when a generic name is used, the label must
also contain the identifier of the manufacturer or distributor;
(6) Directions for use by the
patient;
(7) Name of
practitioner;
(8) Required
precautionary information regarding controlled substances;
(9) Such other and further accessory
cautionary information as required for patient safety;
(10) An expiration date after which the
patient should not use the drug or medicine. Expiration dates on prescriptions
must not exceed:
(a) That on the
manufacturer's container if dispensed in the manufacturer's container;
or
(b) The earliest date of either:
(A) The manufacturer's expiration date;
or
(B) One year from the date the
drug was repackaged and dispensed.
(11) Any drug expiring before the expected
length of time for the course of therapy must not be dispensed.
(12) Any dispensed prescription medication,
other than those in unit dose or unit of use packaging, must be labeled with
its physical description, including any identification code that may appear on
tablets and capsules.
Notes
Statutory/Other Authority: ORS 689.205
Statutes/Other Implemented: ORS 689.505, ORS 689.515 & 2023 SB 450
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