32-1963. Liability of manager, proprietor or
pharmacist in charge of a pharmacy; variances in quality of drugs
or devices prohibited
A. The proprietor, manager, and pharmacist in charge of a pharmacy shall be
responsible for the quality of drugs and devices sold or dispensed in the pharmacy,
except those sold in original packages of the manufacturer.
B. No pharmacist or other person shall manufacture, compound, dispense, or offer
for sale or cause to be manufactured, compounded, dispensed, or offered for sale any drug
or device under or by a name recognized in the official compendium or the federal act
which differs from the standard of strength, purity and quality specified therein as
official at the time of manufacture, compounding, dispensing, or offering for sale, nor
shall a pharmacist or other person manufacture, compound, dispense, or offer for sale, or
cause to be manufactured, compounded, dispensed, or offered for sale, any drug or device,
the strength, purity or quality of which falls below the required strength, purity or
quality under which it is sold.
C. Within four working days of receiving a request, the proprietor, manager or
pharmacist in charge shall provide the following documents relating to the acquisition or
disposal of prescription-only and controlled substance medication if this information is
requested by an authorized board agent in the course of his official duties:
1. Invoices.
2. Stock transfer documents.
3. Merchandise return memos.
4. Other related documentation.
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