NAC639.6702. Records concerning drug products compounded in excess and in bulk quantities.

For each compounded drug product that is in excess of the amount required by the prescription or chart order and each compounded drug product that is compounded in bulk quantities, the pharmacist who compounded or supervised the compounding of the compounded drug product shall prepare a record, either on paper or in the pharmacy’s computer system, that includes, without limitation:

     1. The name of the compounded drug product;

     2. A list of the components and quantities of components used to compound the drug product, including, without limitation, the manufacturer or supplier of the components used, the lot number of the components used and the expiration dates of the components used;

     3. The internal control number assigned to the compounded drug product by the pharmacist or the number of the prescription of the compounded drug product;

     4. The beyond-use date of the compounded drug product;

     5. The date of preparation of the compounded drug product;

     6. The initials of the pharmacist or pharmaceutical technician who compounded the compounded drug product;

     7. If the drug product was compounded by a pharmaceutical technician, the initials of the pharmacist who supervised the pharmaceutical technician; and

     8. The quantity of the final compounded drug product.

     (Added to NAC by Bd. of Pharmacy by R035-06, eff. 9-18-2008)