1. (A) The Department of Health and Environmental Control, Bureau of Drug Control may establish and maintain a program to monitor the prescribing and dispensing of all Schedule II, III, and IV controlled substances by professionals licensed to prescribe or dispense these substances in this State.

2. (B)

   1. (1) A dispenser shall submit to drug control, by electronic means, information regarding each prescription dispensed for a controlled substance. The following information must be submitted for each prescription:

      1. (a) dispenser DEA registration number;
      2. (b) date drug was dispensed;
      3. (c) prescription number;
      4. (d) whether prescription is new or a refill;
      5. (e) NDC code for drug dispensed;
      6. (f) quantity dispensed;
      7. (g) approximate number of days supplied;
      8. (h) patient name;
      9. (i) patient address;
      10. (j) patient date of birth;
      11. (k) prescriber DEA registration number;
      12. (l) date prescription issued by prescriber.
   2. (2) A dispenser shall submit the information required pursuant to subsection (B)(1) in accordance with transmission methods and protocols provided in the "ASAP Telecommunications Format for Controlled Substances, May 1995 Version", developed by the American Society for Automation in Pharmacy, and frequency established by drug control, but shall report at least every thirty days, between the 1st and the 15th of the month following the month the prescription was dispensed.
   3. (3) Drug control may issue a waiver to a dispenser who is unable to submit prescription information by electronic means. The waiver may permit the dispenser to submit prescription information by paper form or other means if all information required pursuant to subsection (B)(1) is submitted in this alternative format.

HISTORY: 2006 Act No. 396, Section 1, eff June 14, 2006.