New Mexico Register / Volume XXXIV, Issue 19 / October 10, 2023

 

 

This is an amendment to 16.19.29 NMAC, Section 7 and 8, effective 10/10/2023.

 

Subsections A through E and G through N of 16.19.29.7 NMAC were not published, as there are no changes. Subsections A and C through D of 16.19.29.8 NMAC were not published, as there are no changes.

 

16.19.29.7             DEFINITIONS:

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                F.            “Drug of concern” means a non-controlled dangerous drug that the Board has by rule determined to require dispenser PMP reporting of in the same manner as controlled substance prescription dispensing, when required reporting is expected to protect patients due to interaction of the drug of concern with controlled substances or other compelling issue. Gabapentin is a drug of concern, except when dispensed pursuant to a prescription issued by a veterinarian.

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[16.19.29.7 NMAC - N, 07/15/2004; A, 06/11/2011; A, 08/31/2012; A, 10/24/2014; A, 03/22/2015; A, 11/27/2016; A, 09/25/2018; A, 2/28/2023, A 10/10/2023]

 

16.19.29.8             MANDATORY REPORTING OF PRESCRIPTION INFORMATION TO THE PMP:

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                B.            Each dispenser shall submit to the board by electronic means information regarding each prescription dispensed for a drug included under Subsection A of this section.  Information to be submitted for each prescription as well as the standards for how this information shall be formatted, not contrary to law, is defined in the PMP data reporting manual available on the state PMP website at http://nmpmp.[org] info shall include at a minimum:

                                (1)           dispenser NPI number;

                                (2)           dispenser NCPDP number;

                                (3)           dispenser DEA number (unless no controlled substances are dispensed and dispenser has no DEA number);

                                (4)           patient name;

                                (5)           patient address;

                                (6)           patient date of birth;

                                (7)           patient gender;

                                (8)           reporting status (new, revised, void);

                                (9)           prescription number;

                                (10)         date prescription written;

                                (11)         refills authorized;

                                (12)         date prescription filled;

                                (13)         refill number;

                                (14)         product ID (NDC) + product ID qualifier;

                                (15)         quantity dispensed;

                                (16)         days’ supply;

                                (17)         drug dosage units;

                                (18)         transmission form of Rx origin;

                                (19)         payment type;

                                (20)         prescriber NPI number; (except veterinarians)

                                (21)         prescriber DEA number (unless prescriber is prescribing a drug of concern and has no DEA number)

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[16.19.29.8 NMAC - N, 07/15/2004; A, 06/11/2011; A, 08/31/2012; A, 03/22/2015; A, 03/23/2016; A, 09/25/2018; A, 2/28/2023; A 10/10/2023]