N.H. Rev. Stat. Ann. § 126-A:89
Definitions
Effective Jun 17, 20252021, 91:45, eff. July 1, 2021; 148:6, eff. July 1, 2021. 2023, 140:8, I, eff. Aug. 29, 2023. 2024, 126:1, eff. Sept. 1, 2024. 2025, 105:1, eff. June 17, 2025.
In this subdivision:
- I. [Repealed.]
- II. "Commissioner" means the commissioner of the department of health and human services.
- III. "Controlled substance" means controlled drugs as defined in RSA 318-B:1, VI.
- IV. "Department" means the department of health and human services, established in RSA 126-A:4.
- V. "Dispense" means to deliver a controlled substance by lawful means and includes the packaging, labeling, or compounding necessary to prepare the substance for such delivery.
VI. "Dispenser" means a person or entity who is lawfully authorized to deliver a schedule II-IV controlled substance, but does not include:
- (a) A licensed hospital pharmacy under RSA 318 that dispenses less than a 48-hour supply of a schedule II-IV controlled substance from a hospital emergency department or that dispenses for administration in the hospital;
- (b) A practitioner, or other authorized person who administers such a substance;
- (c) A wholesale distributor of a schedule II-IV controlled substance or its analog;
- (d) A prescriber who dispenses less than a 48-hour supply of a schedule II-IV controlled substance from a hospital emergency department to a patient;
- (e) A veterinarian who dispenses less than a 48-hour supply of a schedule II-IV controlled substance to a patient; or
(f) A practitioner who does not hold or operate under an active Drug Enforcement Agency registration number to prescribe or dispense controlled substances.
VI-a. "Integrative pain management" means the systematic combination of a variety of allopathic and non-allopathic services that address the biological, psychological, social, and spiritual needs of the patient. It is person-centered and focuses on maximizing function and wellness. Care plans are developed through a shared decision-making model that reflects the available evidence regarding optimal clinical practice and the person's goals and values.
- VII. "Patient" means the person or animal who is the ultimate user of a controlled substance for whom a lawful prescription is issued and for whom a controlled substance or other such drug is lawfully dispensed.
- VIII. "Practitioner" means a physician, dentist, podiatrist, veterinarian, pharmacist, APRN, physician associate, naturopath, or other person licensed or otherwise permitted to prescribe, dispense, or administer a controlled substance in the course of licensed professional practice. "Practitioner" shall also include practitioners with a federal license to prescribe or administer a controlled substance.
- IX. "Prescribe" means to issue a direction or authorization, by prescription, permitting a patient to lawfully obtain controlled substances.
- X. "Prescriber" means a practitioner or other authorized person who prescribes a schedule II, III, or IV controlled substance.
- XI. "Program" means the controlled drug prescription health and safety program that electronically facilitates the confidential sharing of information relating to the prescribing and dispensing of controlled substances listed in schedules II-IV, established by the department pursuant to RSA 126-A:90.
Source. 2021, 91:45, eff. July 1, 2021; 148:6, eff. July 1, 2021. 2023, 140:8, I, eff. Aug. 29, 2023. 2024, 126:1, eff. Sept. 1, 2024. 2025, 105:1, eff. June 17, 2025.