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multistate pharmacy jurisprudence examination — Information & Free Practice

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multistate pharmacy jurisprudence examination

Provider
National Association of Boards of Pharmacy (NABP); appointments scheduled with Pearson
Format
Computer-based adaptive exam with selected-response questions
Exam questions
120
Time limit
2.5 hours
Passing score
Results reported as pass or fail; 5 attempts per jurisdiction
Examination outline
  • Maine Pharmacy Act (32 M.R.S. ch. 117)
  • Board of Pharmacy Rules ch. 1: Definitions
  • Board of Pharmacy Rules ch. 3: Applicability of Rules to Unregistered Facilities
  • Board of Pharmacy Rules ch. 4: Licensure of Pharmacists
  • Board of Pharmacy Rules ch. 4-A: Administration of Drugs and Vaccines and Operation of a Drug or Vaccine Administration Clinic
  • Board of Pharmacy Rules ch. 5: Continuing Pharmacy Education
  • Board of Pharmacy Rules ch. 6-A: Pharmacy Student Internship Programs
  • Board of Pharmacy Rules ch. 7: Licensure and Employment of Pharmacy Technicians
  • Board of Pharmacy Rules ch. 8: Licensure of Retail Pharmacies
  • Board of Pharmacy Rules ch. 9: Registration of Rural Health Centers
  • Board of Pharmacy Rules ch. 10: Registration of Free Clinics
  • Board of Pharmacy Rules ch. 11: Registration of Mail Order Prescription Pharmacies and Licensure of Mail Order Contact Lens Suppliers
  • Board of Pharmacy Rules ch. 12: Licensure of Manufacturers and Wholesalers
  • Board of Pharmacy Rules ch. 13: Operation of Retail Pharmacies
  • Board of Pharmacy Rules ch. 14: Pharmacy Services at Rural Health Centers
  • Board of Pharmacy Rules ch. 15: Operation of Free Clinics
  • Board of Pharmacy Rules ch. 16: Operation of Wholesalers and Manufacturers
  • Board of Pharmacy Rules ch. 17: Operation of Nuclear Drug Outlets
  • Board of Pharmacy Rules ch. 19: Receipt and Handling of Prescription Drug Orders
  • Board of Pharmacy Rules ch. 20: Automated Pharmacy Systems
  • Board of Pharmacy Rules ch. 20-A: Self-Service Customer Kiosks
  • Board of Pharmacy Rules ch. 21: Central Prescription Processing
  • Board of Pharmacy Rules ch. 22: Sale of Schedule V Controlled Substances
  • Board of Pharmacy Rules ch. 23: Accounting for Prescription Drugs
  • Board of Pharmacy Rules ch. 24: Retention of Records by Pharmacies
  • Board of Pharmacy Rules ch. 25: Patient Counseling
  • Board of Pharmacy Rules ch. 26: Generic Substitution
  • Board of Pharmacy Rules ch. 28: Enforcement and Disciplinary Procedures
  • Board of Pharmacy Rules ch. 29: Violations of State or Federal Law or Rule; Other Standards
  • Board of Pharmacy Rules ch. 30: Unprofessional Conduct
  • Board of Pharmacy Rules ch. 31: Practice of Fraud or Deceit
  • Board of Pharmacy Rules ch. 32: Issuance of Citations
  • Board of Pharmacy Rules ch. 33: Access to Certain Medications by Certified Midwives
  • Board of Pharmacy Rules ch. 34: Licensure of Retail Suppliers of Medical Oxygen
  • Board of Pharmacy Rules ch. 35: Licensure of Extended Hospital Pharmacies
  • Board of Pharmacy Rules ch. 37: Licensure of Sterile Compounding Pharmacies
  • Board of Pharmacy Rules ch. 38: Licensure of Closed-Shop Pharmacies
  • Board of Pharmacy Rules ch. 39: Collaborative Drug Therapy Management (joint rule with Board of Licensure in Medicine ch. 5)
  • Board of Pharmacy Rules ch. 39-A: Collaborative Drug Therapy Management (joint rule with State Board of Nursing ch. 1)
  • Board of Pharmacy Rules ch. 40: Authorization, Training and Procedures for Prescribing and Dispensing Naloxone Hydrochloride
  • Board of Pharmacy Rules ch. 41: Sales of Nonprescription Drugs through Vending Machine Outlets
  • Board of Pharmacy Rules ch. 42: Compounding Drugs for Veterinarian Office Use
  • Board of Pharmacy Rules ch. 43: Prescribing, Dispensing and Administering HIV Prevention Drugs
  • Board of Pharmacy Rules ch. 44: Pharmacist Authorization to Make Certain Contraception Accessible
  • 21 CFR Part 1300: Definitions
  • 21 CFR Part 1301: Registration of Manufacturers, Distributors, and Dispensers of Controlled Substances
  • 21 CFR Part 1302: Labeling and Packaging Requirements for Controlled Substances
  • 21 CFR Part 1304: Records and Reports of Registrants
  • 21 CFR Part 1305: Orders for Schedule I and II Controlled Substances
  • 21 CFR Part 1306: Prescriptions
  • 21 CFR Part 1307: Miscellaneous
  • 21 CFR Part 1308: Schedules of Controlled Substances
  • 21 CFR Part 1309: Registration of Manufacturers, Distributors, Importers and Exporters of List I Chemicals
  • 21 CFR Part 1310: Records and Reports of Listed Chemicals and Certain Machines; Importation and Exportation of Certain Machines
  • 21 CFR Part 1311: Requirements for Electronic Orders and Prescriptions
  • 21 CFR Part 1312: Importation and Exportation of Controlled Substances
  • 21 CFR Part 1313: Importation and Exportation of List I and List II Chemicals
  • 21 CFR Part 1314: Retail Sale of Scheduled Listed Chemical Products
  • 21 CFR Part 1316: Administrative Functions, Practices, and Procedures
  • 21 CFR Part 1317: Disposal
  • 21 CFR Part 1321: DEA Mailing Addresses
Examination sources

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