Manufacturer and Distributor Reporting

Every manufacturer and distributor required to register under the provisions of this section shall provide all data required pursuant to 21 U.S.C., Section 827(d)(1) on a monthly basis to the Oklahoma State Bureau of Narcotics and Dangerous Drugs Control. Controlled dangerous substances in Schedule I shall be reported in accordance with rules promulgated by the Director. Reporting of controlled dangerous substances pursuant to 21 U.S.C., Section 827(d)(1) shall include, but not be limited to:

  1. The manufacturer's or distributor's name, address, phone number, DEA  registration number and controlled dangerous substance registration number issued by the Bureau;
  2. The name, address and DEA registration number of the entity to whom the controlled dangerous substance was sold;
  3. The date of the sale of the controlled dangerous substance;
  4. The name and National Drug Code of the controlled dangerous substance sold; and
  5. The number of containers and the strength and quantity of controlled dangerous substances in each container sold.

Pharmaceutical Manufacturers and Distributors can find a user guide: Here. Please submit the above information in accordance with the instructions in the user guide to the following repository: https://pmpclearinghouse.net/opiatereporting/users/sign_in

 

Medical Marijuana Growers, Dispensaries, Processors: continue to complete the OMMA report. We will receive a copy. This is subject to change at any time.

 

All reports are due the 15th day of the following month.