Phar 7.05(2)(h) (h) Prescription order number.

Phar 7.05(2)(i) (i) Quantity.

Phar 7.05(2)(j) (j) Number of refills or quantity remaining.

Phar 7.05(2)(k) (k) Directions for use of the prescribed drug or device as contained in the prescription order.

Phar 7.05(3) (3) A label for prescribed drugs or devices may include the following:

Phar 7.05(3)(a) (a) Symptom or purpose for which the drug is being prescribed if requested by the patient.

Phar 7.05(3)(b) (b) Both the generic name of the drug product equivalent and the brand name specified in the prescription order may be listed on the label if the brand name is listed on the prescription and the drug product equivalent is dispensed, unless the prescribing practitioner requests that the brand name be omitted from the label.

Phar 7.05(3)(c) (c) Written or graphic product descriptions.

Phar 7.05(3)(d) (d) Any cautions or other provisions.

Phar 7.05(4) (4) Subsection (2) does not apply to complimentary samples of drug products or devices dispensed in original packaging by a practitioner to his or her patients.

Phar 7.05 History History: CR 19-145: cr. Register December 2020 No. 780, eff. 1-1-21.

Phar 7.06 Phar 7.06 Repackaging for stock. A pharmacy repackaging for stock any non-sterile drugs shall do all of the following:

Phar 7.06(1) (1) The repackaging for stock process is conducted under conditions that ensure the integrity of the drug.

Phar 7.06(2) (2) Products repackaged for stock shall include a beyond use date that ensures the integrity of the drug.

Phar 7.06(3) (3) The repackaged container shall be selected to mitigate adulteration from light, temperature and humidity.

Phar 7.06(4) (4) The repackaged for stock drugs are labeled physically or electronically with all the following components:

Phar 7.06(4)(a) (a) Drug name, strength, form and beyond use date.

Phar 7.06(4)(b) (b) One of the following identifiers:

Phar 7.06(4)(b)1. 1. Pharmacy control number.

Phar 7.06(4)(b)2. 2. NDC number and manufacturer lot number.

Phar 7.06(4)(b)3. 3. Name of manufacturer or distributer of the drug product, and the manufacturer lot number.

Phar 7.06(5) (5) Records of all repackaging for stock operations are maintained and include all the following:

Phar 7.06(5)(a) (a) Name, strength, form, quantity per container, and quantity of containers.

Phar 7.06(5)(b) (b) NDC number or the name of the manufacturer or distributor of the drug product.

Phar 7.06(5)(c) (c) Manufacturer lot number.

Phar 7.06(5)(d) (d) Original container’s expiration date and the beyond-use date for the new containers.

Phar 7.06(5)(e) (e) First and last name of the pharmacist or delegate that repackaged the drug and the first and last name of the pharmacist that verified the accuracy of the repackaging.

Phar 7.06(5)(f) (f) Date of repackaging.

Phar 7.06(5)(g) (g) Any pharmacy control numbers.