1. (a) If a patient requests a transfer of their prescription, a copy of the original prescription shall be transmitted upon the request of the receiving pharmacist.

2. (b) The information included in the transfer of the prescription shall include:

   1. (1) Active ingredient(s),
   2. (2) Concentration,
   3. (3) Dosage Form e.g. capsule, cream, suspension, injectable, etc.
   4. (4) Route of delivery e.g. oral, injectable, topical, vaginal, etc.
   5. (5) Delivery mechanism e.g. topical, transdermal, immediate release, sublingual, etc.
   6. (6) Dosing Duration e.g. Q12H, Q24H, Q72H, etc.
   7. (7) Details about the compounding procedure must be reasonably available from the transferring pharmacy.

Added at 26 Ok Reg 2276, eff 7-1-09