Oregon § 689.813 Exemption from drug labeling requirements

Oregon Statutes

§ 689.813 — Exemption from drug labeling requirements

Oregon § 689.813

Vol.17

Title 52Occupations and Professions

Ch. 689Pharmacists; Drug Outlets; Drug Sales

This text of Oregon § 689.813 (Exemption from drug labeling requirements) is published on Counsel Stack Legal Research, covering Oregon primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

Or. Rev. Stat. § 689.813 (2026).

Text

(1)A requirement that a health care provider who is authorized to prescribe drugs in this state label a drug dispensed by the health care provider with the information described in subsection (2) of this section does not apply to a drug approved by the United States Food and Drug Administration for the reversal of an opioid overdose if the drug is:

(a)In the form of a nasal spray; and

(b)Personally dispensed by a health care provider described in this subsection at the location of practice of the health care provider.

(2)The information described in subsection (1) of this section includes:

(a)The name of the patient;

(b)The name and address of the dispensing health care provider;

(c)The date of dispensing;

(d)(A) The name of the drug or, if the dispensed drug does not have a brand n

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(1) A requirement that a health care provider who is authorized to prescribe drugs in this state label a drug dispensed by the health care provider with the information described in subsection (2) of this section does not apply to a drug approved by the United States Food and Drug Administration for the reversal of an opioid overdose if the drug is:
(a) In the form of a nasal spray; and
(b) Personally dispensed by a health care provider described in this subsection at the location of practice of the health care provider.
(2) The information described in subsection (1) of this section includes:
(a) The name of the patient;
(b) The name and address of the dispensing health care provider;
(c) The date of dispensing;
(d)(A) The name of the drug or, if the dispensed drug does not have a brand name, the generic name of the drug along with the name of the drug distributor or manufacturer;
(B) The drug’s quantity per unit, unless the drug is a compound; and
(C) The directions for the drug’s use stated in the prescription;
(e) Cautionary statements, if any, as required by law; and
(f) When applicable and as determined by the State Board of Pharmacy, an expiration date after which the patient should not use the drug.