Maine Revised Statutes
Subchapter 9: MISCELLANEOUS PROVISIONS
32 §13800-C. Opioid medication product registration fee

§13800-C. Opioid medication product registration fee
(CONTAINS TEXT WITH VARYING EFFECTIVE DATES)
This section governs opioid medication product registration fees. As used in this section, "unit of an opioid medication" means the lowest identifiable quantity of the opioid medication that is dispensed.   [PL 2019, c. 536, §4 (NEW).]
1.  Registration fee.  Except as provided in subsection 2, a manufacturer that sells, delivers or distributes an opioid medication in this State shall pay an annual registration fee of $250,000 to the board on December 31st of each year.  
[PL 2019, c. 536, §4 (NEW).]
2.  Exception.  A manufacturer that does not sell, deliver or distribute 2,000,000 or more units of an opioid medication within this State in the year in which a registration fee is due is not required to pay the registration fee. To qualify for the exception under this subsection, a manufacturer must demonstrate to the board, by January 31st of the year following the year in which the registration fee is due, in a manner determined by the board, that the manufacturer did not sell, deliver or distribute 2,000,000 or more units of an opioid medication within this State in the year in which the manufacturer seeks to claim the exception. The board may adopt rules to implement this section. Rules adopted pursuant to this subsection are routine technical rules as defined in Title 5, chapter 375, subchapter 2‑A.  
[PL 2019, c. 536, §4 (NEW).]
3.  Calculation of units of an opioid medication sold, delivered or distributed.  When calculating the number of units of an opioid medication sold, delivered or distributed by a manufacturer under subsection 2, units of an opioid medication may be excluded when prescribed for the purpose of medication-assisted treatment of substance use disorder. The board periodically shall provide to the Department of Health and Human Services a list of medications exempted under this subsection.  
[PL 2019, c. 536, §4 (NEW).]
4.  (TEXT EFFECTIVE UNTIL 9/1/23) (TEXT REPEALED 9/1/23) Registration fee review and report.  By March 1st of each year following calendar years 2020, 2021 and 2022, the board shall evaluate and report whether the registration fee due under this section and the fee due under section 13724 have affected the prescribing practices of opioid medications by reducing the number of opioid medication prescriptions issued during calendar years 2020, 2021 and 2022 or whether the fees have created any unintended consequences in the availability of opioid medications for the treatment of chronic or intractable pain, to the extent the board has the ability to identify a correlation. The board shall provide the report to the joint standing committee of the Legislature having jurisdiction over health and human services matters, which may report out legislation based upon the report.  
This subsection is repealed September 1, 2023.  
[PL 2019, c. 536, §4 (NEW).]
SECTION HISTORY
PL 2019, c. 536, §4 (NEW).

Structure Maine Revised Statutes

Maine Revised Statutes

TITLE 32: PROFESSIONS AND OCCUPATIONS

Chapter 117: MAINE PHARMACY ACT

Subchapter 9: MISCELLANEOUS PROVISIONS

32 §13781. Generic and therapeutically equivalent substitution

32 §13782. Advertising

32 §13782-A. Price disclosure

32 §13783. Posting prices (REPEALED)

32 §13784. Patient information regulation

32 §13785. Patient profile record system regulation

32 §13786. Identification of persons prescribing medicines on hospital prescription blanks

32 §13786-A. Security requirements; rules

32 §13786-B. Partial dispensing of prescription for opioid medication

32 §13786-C. Dispensing of prescription of opioid medication; immunity

32 §13786-D. Prescribing and dispensing insulin

32 §13786-E. Prescribing, dispensing and administering HIV prevention drugs

32 §13786-F. Dispensing of emergency supplies of chronic maintenance drug

32 §13787. Hypodermic syringes; prescriptions (REPEALED)

32 §13787-A. Sale of hypodermic apparatus

32 §13788. Sale of poisonous drugs

32 §13789. Possession of drug samples

32 §13790. Using drugs not in prescription

32 §13791. Return of drugs

32 §13792. Sale by certain methods prohibited

32 §13793. Adulterating and selling drugs

32 §13794. Labeling of prescriptions

32 §13795. Photographic proof of identification; discretion to sell or dispense; immunity

32 §13796. Retail sale of targeted methamphetamine precursors

32 §13797. Prescription drug price information

32 §13798. Expedited partner therapy

32 §13799. Consumer choice preserved

32 §13800. Access to distributed drugs

32 §13800-A. Liability for product of another; exemption

32 §13800-B. Prohibition on providing conversion therapy to minors

32 §13800-C. Opioid medication product registration fee

32 §13800-D. Insulin product registration fee (WHOLE SECTION TEXT EFFECTIVE UNTIL 1/01/27) (WHOLE SECTION TEXT REPEALED 1/01/27)