North Carolina General Statutes
Article 4A - North Carolina Pharmacy Practice Act.
§ 90-85.27 - Definitions.

90-85.27. Definitions.
As used in G.S. 90-85.28 through G.S. 90-85.31:
(1) Biological product. - As defined in section 351(i) of the Public Health Service Act, 42 U.S.C. 262(i).
(1a) Equivalent drug product. - A drug product which has the same established name, active ingredient, strength, quantity, and dosage form, and which is therapeutically equivalent to the drug product identified in the prescription.
(2) Established name. - As defined in section 502(e)(3) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. 352(e)(3).
(3) Good manufacturing practice. - As defined in Part 211 of Chapter 1 of Title 21 of the Code of Federal Regulations.
(3a) Interchangeable biological product. - A biological product determined by the United States Food and Drug Administration to meet the standards set forth in 42 U.S.C. 262(k)(4), or deemed therapeutically equivalent by the United States Food and Drug Administration.
(4) Manufacturer. - The actual manufacturer of the finished dosage form of the drug.
(4a) Narrow therapeutic index drugs. - Those pharmaceuticals having a narrowly defined range between risk and benefit. Such drugs have less than a twofold difference in the minimum toxic concentration and minimum effective concentration in the blood or are those drug product formulations that exhibit limited or erratic absorption, formulation-dependent bioavailability, and wide intrapatient pharmacokinetic variability that requires blood-level monitoring. Drugs identified as having narrow therapeutic indices shall be designated by the North Carolina Secretary of Health and Human Services upon the advice of the State Health Director, North Carolina Board of Pharmacy, and North Carolina Medical Board, as narrow therapeutic index drugs and shall be subject to the provisions of G.S. 90-85.28(b1). The North Carolina Board of Pharmacy shall submit the list of narrow therapeutic index drugs to the Codifier of Rules, in a timely fashion for publication in January of each year in the North Carolina Register.
(5) Prescriber. - Anyone authorized to prescribe drugs pursuant to the laws of this State. (1979, c. 1017, s. 1; 1981 (Reg. Sess., 1982), c. 1188, s. 3; 1983, c. 196, s. 9; 1997-76, s. 1; 1997-443, s. 11A.118(b); 2015-27, s. 1.)

Structure North Carolina General Statutes

North Carolina General Statutes

Chapter 90 - Medicine and Allied Occupations

Article 4A - North Carolina Pharmacy Practice Act.

§ 90-85.2 - Legislative findings.

§ 90-85.3 - Definitions.

§ 90-85.3A - Practice of pharmacy.

§ 90-85.4 - North Carolina Pharmaceutical Association.

§ 90-85.5 - Objective of Pharmaceutical Association.

§ 90-85.6 - Board of Pharmacy; creation; membership; qualification of members.

§ 90-85.7 - Board of Pharmacy; selection; vacancies; commission; term; per diem; removal.

§ 90-85.8 - Organization.

§ 90-85.9 - Meetings.

§ 90-85.10 - Employees; Executive Director.

§ 90-85.11 - Compensation of employees.

§ 90-85.11A - Acquisition of real property; equipment; liability insurance.

§ 90-85.12 - Executive Director to make investigations and prosecute.

§ 90-85.13 - Approval of schools and colleges of pharmacy.

§ 90-85.14 - Practical experience program.

§ 90-85.15 - Application, qualifications, and criminal record check for licensure as a pharmacist; prerequisites.

§ 90-85.15A - Pharmacy technicians.

§ 90-85.15B - Immunizing pharmacists.

§ 90-85.16 - Examination.

§ 90-85.17 - License renewal.

§ 90-85.18 - Approval of continuing education programs.

§ 90-85.19 - Reinstatement.

§ 90-85.20 - Licensure without examination.

§ 90-85.21 - Pharmacy permit.

§ 90-85.21A - Applicability to out-of-state operations.

§ 90-85.21B - Unlawful practice of pharmacy.

§ 90-85.21C - Pharmacy permit exemption for dispensing and delivery of home renal products.

§ 90-85.21D - Dialysis facilities as designated agents to receive home medications for patients with renal failure.

§ 90-85.22 - Device and medical equipment permits; exemptions.

§ 90-85.23 - License and permit to be displayed.

§ 90-85.24 - Fees collectible by Board.

§ 90-85.25 - Disasters and emergencies.

§ 90-85.26A - Clinical pharmacist practitioners subcommittee.

§ 90-85.27 - Definitions.

§ 90-85.28 - Selection by pharmacists permissible; prescriber may permit or prohibit selection; price limit on selected drugs; communication of dispensed biological products under specified circumstances.

§ 90-85.29 - Prescription label.

§ 90-85.30 - Prescription record.

§ 90-85.31 - Prescriber and pharmacist liability not extended.

§ 90-85.32 - Rules pertaining to filling, refilling, transfer, and mail or common-carrier delivery of prescription orders.

§ 90-85.33 - Unit dose medication systems.

§ 90-85.34 - Unique pharmacy practice.

§ 90-85.34A - Public health pharmacy practice.

§ 90-85.35 - Availability of patient records.

§ 90-85.36 - Availability of pharmacy records.

§ 90-85.37 - Embargo.

§ 90-85.38 - Disciplinary authority.

§ 90-85.39 - Injunctive authority.

§ 90-85.40 - Violations.

§ 90-85.41 - Board agreements with special peer review organizations for impaired pharmacy personnel.

§ 90-85.44 - Drug, Supplies, and Medical Device Repository Program established.