New Jersey Multistate Pharmacy Jurisprudence Examination (MPJE) Practice Exam

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• What should be done with a DEA 222 Form that contains a mistake?
• What is the blanket authorization for destruction of controlled substances?
• Which act is violated if a pharmacist dispenses a recalled medication?
• What distinguishes Class III devices from Class I and II devices?
• If a pharmacy has zero inventory at the start, what is required?
• Are logbook records for pseudoephedrine required to be kept for the same duration as CV and opium sales?
• Can a physician write a prescription for an animal?
• How much pseudoephedrine can be sold without requiring a logbook entry?
• How long is Maintenance Treatment for substance use?
• What information must the transferee pharmacist include on the prescription after a transfer?
• What is the maximum number of 30mg pseudoephedrine tablets a person can buy in one day?
• Which group does Clozaril (clozapine) require pharmacies to register with?
• Under what condition can a practitioner prescribe a 90-day supply of a CII medication?
• What is one requirement for faxing prescriptions for a long-term care facility?
• Can a pharmacist deny access to an FDA inspector?
• Which type of prescriptions are exempt from the standard refill regulations for CII drugs?
• What should a pharmacy employee do if they encounter a data breach?
• Can you erase a mistake made on a DEA 222 form?
• Is it permissible to fax a CII prescription?
• How quickly must a pharmacy report a theft or significant loss of controlled substances to the DEA?
• Can a pharmacist allow the use of a drug for an off-label use?
• What is required for a pharmacist to note when processing additional refills on a CIII-CV prescription?
• Which act formalized the regulations for drug disposal methods?
• What does a drug contain that can lead to it being labeled dangerous or adulterated?
• What is the primary function of a pharmacy designated as a "collector"?
• What information is required on a prescription for an animal?
• What is the requirement for CIII-CV prescriptions during inventory?
• What is the required registration frequency for distributors with the Attorney General?
• What are the two drug classes that mandate a package insert?
• What is one criterion that requires a pharmacy to perform an inventory count?
• Which of the following is the generic name for Lotronex?
• Whose responsibility is it to ensure a drug is correctly labeled?
• In New Jersey, what must a pharmacy designated as a "collector" do within 5 days of receiving that designation?
• How long should written patient acknowledgment of the Notice of Private Practices be retained by the pharmacy?
• What is the expiration timeframe for CIII - CV prescriptions after issuance?
• Are all acetaminophen and aspirin containers required to have child-resistant packaging?
• Where can individuals safely dispose of extra oxycodones?
• How many partial fillings are permitted on a CIII prescription?
• Can pharmacies accept phone or electronic prescriptions for Lotronex?
• How much pseudoephedrine can be purchased over the mail in 30 days?
• What did the Durham Humphrey Amendment establish?
• What must the purchaser do if the loss of controlled substances occurs?
• What is the maximum days supply for a CII drug that can be dispensed?
• Does the DCU need to be informed about any loss or theft of controlled substances?
• What was the primary focus of the Food and Drug Administration Modernization Act (FDAMA)?
• What information is vital to maintain for controlled substances in emergency kits?
• What information must be recorded upon receiving a delivery through the CSOS?
• In New Jersey, what additional form is required for lost or stolen controlled substances?
• In a prescription label, which of the following needs to stand out more than other elements?
• How much OTC CV medication, such as codeine, can be sold within a 48-hour period?
• What age must someone be to purchase Plan B (levonorgestrel) without a prescription?
• Which controlled substances must be counted exactly during inventory?
• Which agency regulates the advertising of over-the-counter (OTC) drugs?
• Who must be trained on HIPAA regulations in a pharmacy?
• What primary change did the Waxman Hatch Amendment facilitate regarding generic drugs?
• What does REMS stand for in the context of pharmaceutical regulations?
• What must certain healthcare facilities establish to be authorized to dispose of controlled substances?
• What is a specific requirement for labeling commercial packages of controlled substances in New Jersey?
• What is the DEA 41 Form used for?
• What is included in the Drug Facts Panel for OTC products?
• How often must a pharmacy register with the Attorney General?
• In the two-drawer method for filing prescriptions, what must CIII-CV drugs have?
• What is considered an emergency situation under which a prescriber can provide a CII prescription?
• What defines long-term detoxification in relation to time?
• What identification is required to purchase a CV OTC drug?
• When must a pharmacy conduct controlled substances inventory counts?
• The term "CSOS coordinator" refers to which role in a pharmacy?
• What regulatory requirement exists for pharmacists dispensing medications subject to REMS?
• What is the maximum amount of controlled substances a pharmacy can transfer without registering as a distributor?
• What is the maximum amount of medication that can be prescribed in an emergency CII prescription?
• What must a transmitting pharmacy do when sending a prescription to a central fill pharmacy?
• What is required for pharmacies that sell controlled substances online under the Ryan Haight Act?
• What distinguishes the DEA 224a Form from the DEA 224 Form?
• What claims are dietary supplements prohibited from making?
• For how long must controlled substances refill information be retained?
• When can an FDA inspector conduct an inspection without a search warrant?
• What does a hyphen in a DEA number indicate?
• What does the Ryan Haight Online Pharmacy Consumer Protection Act aim to address?
• What type of devices fall under Class II according to regulatory standards?
• What happens to the copies of the DEA 222 Form?
• Can a pharmacy intern take down a prescription?
• Which act requires drugs to be marked as safe and have adequate usage directions?
• What are Good Manufacturing Practices?
• Who is responsible for reporting a loss of controlled substances after the shipment has been received?
• Is there an age requirement for purchasing pseudoephedrine in New Jersey?
• How long must pharmacy inventory records be kept?
• Which entity is responsible for enforcing HIPAA regulations?
• What is the maximum beyond-use date for a multidose vial?
• What is a significant consequence of non-compliance with HIPAA standards?
• For whom is the special agent's approval significant in drug disposal?
• What is a requirement for labeling drugs under the Food, Drug, and Cosmetics Act?
• Who is legally permitted to prescribe medication for animals?
• What form is required to dispense CII drugs from a prescriber to a pharmacy?
• Can a faxed prescription be considered the original for CIII - CV?
• What action is required from patients when pharmacies implement new privacy practices?
• What is the purpose of a DEA 106 Form?
• Is the inclusion of questions and a telephone number in the Drug Facts Panel mandatory for OTC drugs?
• What does the acronym NDC stand for?
• What is the penalty for committing robbery resulting in death?
• For how long must CSOS records be maintained?
• Which of the following is NOT a requirement under the Notice of Privacy Practices?
• For how long should logbook records for CV and opium sales be maintained?
• What must be included on the label from a central fill pharmacy?
• What is the maximum duration for short-term detoxification?
• Who is primarily responsible for deciding the schedule in which a drug falls?
• Which insulin brands typically do not require a prescription?
• What is the maximum amount of pseudoephedrine one can purchase in 30 days?
• Can a practitioner authorize additional refills on a CIII-CV oral refill authorization?
• What distinguishes recoverable damaged controlled substances from non-recoverable ones?
• Who can request a blanket waiver for non-child resistant packaging?
• What could potentially lead to a label being deemed misleading?
• What is one consequence of using a drug that is made in unsanitary conditions?
• What is the role of the FTC regarding OTC drug advertising?
• What letters can a DEA number for a Type A practitioner start with?
• What is the maximum amount of pseudoephedrine one can purchase in a single day?
• What must be included in the documentation for the transfer by the transferring pharmacist?
• What is one of the key purposes of the Kefauver Harris Amendment?
• Is a digital certificate required to start ordering through CSOS?
• After administering an emergency CII prescription, how long does the prescriber have to provide a hard copy to the pharmacist?
• Can a CII be mailed to a patient?
• What type of information does the pseudoephedrine sales logbook record?
• Which type of pharmacy can destroy controlled substances on-site if modification is made?
• What must a pharmacy do when a drug is just scheduled?
• Are hospitals required to report to the prescription monitoring program?
• Can all pharmacies destroy controlled substances on-site?
• Can a pharmacy perform inventory on a date different from its regular biennial inventory date?
• What is the maximum number of refills allowed on a CIII - CV prescription?
• Are partial fillings allowed for CIII-CV prescriptions?
• How often must pharmacies conduct a risk assessment for HIPAA compliance?
• How many grams of pseudoephedrine can one person purchase per day?
• For how long must entries in the pseudoephedrine logbook be retained?
• What should the purchaser do if they receive a partial order from a supplier?
• What is the purpose of the DEA 224 Form?
• What phrase must be included on the hard copy of an emergency CII prescription?
• What details must be recorded on copy 3 of the DEA 222 Form?
• What is required of a registrant to use CSOS?
• Is it a legal requirement to lock up controlled substances in pharmacies?
• What should pharmacies do with complaints regarding privacy practices?
• Who receives an exception to controlled substances labeling requirements?
• How much base pseudoephedrine is contained in a 30mg tablet?
• Which of the following must be included on every prescription label?
• What key information must be accurate on a drug label to avoid being misbranded?
• What packaging requirement does the NDC not need to meet for bulk packaging?
• Is it mandatory to file with a red "C" for prescriptions?
• Which of the following is NOT a criterion for a drug to be considered adulterated?
• What is the specific REMS program name for Lotronex (alosetron)?
• Are electronically transmitted CII - CV prescriptions allowed?
• Which of the following conditions can result in a drug being classified as both adulterated and misbranded?
• What happens if a pharmacy fails to contact the DEA after an emergency CII prescription?
• What must a transferring pharmacist do regarding the prescription during a transfer process?
• What is the expiration period for a CII prescription after it has been issued?
• Which of the following is a requirement for drug labeling under the law?
• Who is responsible for signing the DEA 222 form?
• Which medications can exceed the 30-day supply limit when prescribed?
• What is one reason a drug can be considered misbranded?
• Is the Orange Book considered federal law?
• Which drug is part of the "No Blood, No Drug" REMS program?
• Can Suboxone and Subutex be dispensed at a retail pharmacy?
• Who can ask for non-child resistant packaging?
• What is the requirement for the labeling of the inner container of a mailed CII?
• How must the symbol indicating the schedule of a controlled substance be presented on a label?
• What is the primary purpose of REMS programs?
• What must a physician check before writing a CII prescription for a new patient?
• What are the conditions for selling a CV OTC drug?
• What is required for Class III medical devices before marketing?
• What must a transferring pharmacist write on the prescription during a transfer?
• If a supplier cancels part of an order, what must they do?
• If a supplier cannot fully fill an order, how long do they have to complete the rest?
• Can a pharmacy sell pseudoephedrine without supervision from a pharmacist or intern?
• What condition may indicate that a drug’s strength or quality is compromised?
• Which class of medical device has the least regulation?
• What is the consequence of not notifying the DEA when performing inventory on a date other than the biennial date?
• Who is responsible for the oversight of prescription drug advertising?
• What information must be recorded in the logbook for pseudoephedrine sales?
• What is the maximum number of years a pharmacy can retain patient acknowledgment records under HIPAA guidelines?
• Which group must obtain a prescription for Plan B (levonorgestrel)?
• Can prescription vials be reused according to current regulations?
• What does CSOS stand for in relation to pharmacy law?
• Can a non-employee submit a CII prescription to a pharmacist?
• How many times can a scheduled drug be transferred between pharmacies that do not share a database?
• What quantity limit is placed on emergency kits in long-term care facilities?
• Where must pseudoephedrine be located in a pharmacy?
• Can a pharmacist refuse an inspection if the inspector has only a Notice of Inspection?
• What can a purchaser do if they want to cancel part of an order?
• Is it permissible to dispense methadone for the treatment of addiction?
• Can a pharmacist dispense a CII prescription if it is missing the prescriber's DEA number?
• Under what conditions can a long-term care facility have controlled substances on hand?
• What must OTC products have that is similar to prescription drugs?
• What happens if a pharmacy does not maintain CSOS records for the required time?
• Under what circumstances is a drug considered adulterated?
• What can patients request regarding their health information under HIPAA?
• How frequently does a manufacturer need to register with the Attorney General?
• What is required for the dispensing of controlled substances from retail pharmacies?
• What must pharmacies do to comply with HIPAA regulations regarding patient information?
• What is the maximum amount of opium that can be sold OTC within 48 hours?
• How long does a pharmacy have to enter a dispensed drug into the Prescription Monitoring Program?
• Can the FDA itself initiate a recall on a drug?
• What is the primary purpose of the Notice of Privacy Practices?
• Which medication is associated with the S.T.E.P.S. REMS program?