Within seven days after the date a controlled substance prescription is dispensed, a pharmacy must electronically submit to the board the following data elements from all dispensed controlled substance prescriptions:

1. (1) the prescribing practitioner's DEA registration number including the prescriber's identifying suffix of the authorizing hospital or other institution's DEA number when applicable;
2. (2) the official prescription form control number if dispensed from a written official prescription form, unless the prescription is electronic and meets the requirements of Code of Federal Regulations, Title 21, Part 1311;
3. (3) the board's designated placeholder entered into the control number field if the prescription is electronic;
4. (4) the patient's name, age or date of birth, and address including city, state, and zip code; or such information on the animal's owner if the prescription is for veterinarian services;
5. (5) the date the prescription was issued and dispensed;
6. (6) the NDC # of the controlled substance dispensed;
7. (7) the quantity of controlled substance dispensed;
8. (8) the pharmacy's prescription number; and
9. (9) the pharmacy's DEA registration number.

Source Note:The provisions of this §315.6 adopted to be effective March 10, 2016, 41 TexReg 1690.