Okla. Admin. Code § 535:15-9-9

Current through Vol. 42, No. 4, November 1, 2024

Section 535:15-9-9 - Drug distribution and control

(a)Labeling.Each preparation dispensed to patients by a sterile compounding preparation pharmacy shall be labeled with the following information with a permanent label:

(1) Name, address, and telephone number of the pharmacy;

(2) Date and prescription number;

(3) Patient's name;

(4) Name, strength, and amount of each drug;

(5) Directions for use, including infusion rate where applicable;

(6) Prescriber's name;

(7) Required controlled substance transfer warnings, where applicable;

(8) Date of compounding;

(9) Expiration date and time;

(10) Identity of pharmacist compounding and dispensing;

(11) Storage requirements;

(12) Auxiliary labels, where applicable;

(13) Hazardous drug auxiliary labels, where applicable.

(b)Delivery service.The pharmacy manager shall assure the environmental control of all products shipped. Therefore, any compounded sterile preparation or pharmaceutical must be shipped in appropriate containers to insure minimal temperature fluctuation (as defined by USP standards), and stored appropriately in the patient's home. Chain of possession for the delivery of Schedule II controlled substances via courier must be documented.

(c)Disposal of infectious waste.The pharmacy manager is responsible for assuring that there is a system for the disposal of infectious waste in a manner so as not to endanger the public health.

Okla. Admin. Code § 535:15-9-9

Amended at 9 Ok Reg 2141, eff 6-11-92

Amended by Oklahoma Register, Volume 32, Issue 23, August 17, 2015, eff. 8/27/2015.