Regulation of Manufacturing, Distributing, Prescribing, Administering, and Dispensing Controlled Substances | MidpageRegulation of Manufacturing, Distributing, Prescribing, Administering, and Dispensing Controlled Substances
21-28-3.01Rules and regulations — Fees21-28-3.02Registration requirements21-28-3.03Registration21-28-3.04Suspension or revocation of registration21-28-3.05Order to show cause21-28-3.06License required for manufacture21-28-3.07Qualifications for licensees21-28-3.08Disposition of license fees21-28-3.09Denial, revocation, or suspension of licenses21-28-3.10Authorized sales by manufacturers and wholesalers on official written orders21-28-3.11Form, delivery, and preservation of official written orders21-28-3.12Records of controlled substances used in professional practice21-28-3.13Records of manufacturers and wholesalers21-28-3.14Records of apothecaries21-28-3.15Records of vendors of schedule V substances21-28-3.16Form, content, and preservation of records21-28-3.17Records open to inspection21-28-3.18Prescriptions21-28-3.19Sale of stock on discontinuance of pharmacy business21-28-3.20Authority of practitioner to prescribe, administer, and dispense21-28-3.20.1Authority of practitioner to prescribe, administer, and dispense — Cancer, palliative care, and chronic intractable pain21-28-3.21Operation of treatment and rehabilitation programs for drug dependent persons21-28-3.22Administration, dispensation or use restricted to scope of employment or duty21-28-3.23Advertising controlled substances21-28-3.24Examination before use of controlled substances21-28-3.25Subpoena powers21-28-3.26Labeling by manufacturers and wholesalers21-28-3.27Labeling by dispensing apothecaries21-28-3.28Security requirements generally21-28-3.30Persons exempt from restrictions on possession of controlled substances21-28-3.31Use of imitation controlled substance in research — Immunity21-28-3.33Voluntary non-opiate directive form