OAR 855-041-1130
Prescription Labeling
(1)
Prescriptions must be labeled with the following information:(a)
Name, address and telephone number of the pharmacy;(b)
Date;(c)
Identifying number;(d)
Name of patient;(e)
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;(f)
Directions for use by the patient;(g)
Name of practitioner;(h)
Required precautionary information regarding controlled substances;(i)
Such other and further accessory cautionary information as required for patient safety;(j)
An expiration date after which the patient should not use the drug or medicine. Expiration dates on prescriptions must be the same as that on the original container unless, in the pharmacist’s professional judgment, a shorter expiration date is warranted. Any drug bearing an expiration date shall not be dispensed beyond the said expiration date of the drug; and(k)
Any dispensed prescription medication, other than those in unit dose or unit of use packaging, shall be labeled with its physical description, including any identification code that may appear on tablets and capsules.(l)
Upon written request and for good cause, the Board may waive any of the requirements of this rule. A waiver granted under this section shall only be effective when it is issued by the Board in writing.
Source:
Rule 855-041-1130 — Prescription Labeling, https://secure.sos.state.or.us/oard/view.action?ruleNumber=855-041-1130.