§ 21-28-3.01. Rules and regulations — Fees.
§ 21-28-3.02. Registration requirements.
§ 21-28-3.04. Suspension or revocation of registration.
§ 21-28-3.05. Order to show cause.
§ 21-28-3.06. License required for manufacture.
§ 21-28-3.07. Qualifications for licensees.
§ 21-28-3.08. Disposition of license fees.
§ 21-28-3.09. Denial, revocation, or suspension of licenses.
§ 21-28-3.10. Authorized sales by manufacturers and wholesalers on official written orders.
§ 21-28-3.11. Form, delivery, and preservation of official written orders.
§ 21-28-3.12. Records of controlled substances used in professional practice.
§ 21-28-3.13. Records of manufacturers and wholesalers.
§ 21-28-3.14. Records of apothecaries.
§ 21-28-3.15. Records of vendors of schedule V substances.
§ 21-28-3.16. Form, content, and preservation of records.
§ 21-28-3.17. Records open to inspection.
§ 21-28-3.19. Sale of stock on discontinuance of pharmacy business.
§ 21-28-3.20. Authority of practitioner to prescribe, administer, and dispense.
§ 21-28-3.21. Operation of treatment and rehabilitation programs for drug dependent persons.
§ 21-28-3.22. Administration, dispensation or use restricted to scope of employment or duty.
§ 21-28-3.23. Advertising controlled substances.
§ 21-28-3.24. Examination before use of controlled substances.
§ 21-28-3.25. Subpoena powers.
§ 21-28-3.26. Labeling by manufacturers and wholesalers.
§ 21-28-3.27. Labeling by dispensing apothecaries.
§ 21-28-3.28. Security requirements generally.
§ 21-28-3.30. Persons exempt from restrictions on possession of controlled substances.
§ 21-28-3.31. Use of imitation controlled substance in research — Immunity.