FPGEE Management Practice Exam

These questions are part of the practice quiz. Start practicing

• Which entities are required to register to prescribe or dispense isotretinoin?
• Can manufacturers of prescription drugs distribute information about off-label uses of their products?
• How may a physician prescribe a schedule II controlled substance for a hospice patient?
• What specific warning must be included on labels of OTC products for systemic use?
• What does the abbreviation GMP stand for in pharmaceutical manufacturing?
• Which of the following is a Schedule IV controlled substance?
• How often must hospital inpatients receiving oral estrogen therapy receive patient package inserts?
• What is a requirement for the labeling of prescription drugs?
• What does NDC stand for in pharmaceutical terms?
• Which of the following is an approved treatment for narcotic dependence?
• What information must be included on a prescription drug label according to regulations?
• What is true about Schedule V substances?
• Which regulation governs the handling of controlled substances in pharmacy practice?
• How long before a pharmacy technician must perform verification of the contents of unit dose carts?
• If a pharmacist observes a misleading advertisement for a prescription drug, which office should they file a complaint with?
• What must be imprinted on each commercial oral tablet?
• What form must a community pharmacy use to purchase grain alcohol for compounding purposes?
• When considering a purchase of a two-year supply of a popular antibiotic, which of the following is a legal activity?
• Which sublingual tablets do NOT require dispensing in child-resistant containers?
• If a prescription is originally filled on December 1, 2013, and it has refills, what is the earliest refill date allowed?
• Which type of OTC product is required to be in a tamper-resistant package?
• What does the symbol "RLD" in the Electronic Orange Book represent?
• Which product type in a hospital pharmacy must always have a barcode?
• Which statement is true regarding pharmacies handling refills?
• Why might a pharmacist refuse to fill a prescription?
• Which of the following are examples of Schedule I substances?
• What should a pharmacist do if she recognizes a prescription's drug indication as unrecognized but reported in the news?
• In the event of a conviction, how long do you have to notify the Board of Pharmacy?
• Which act was the first to require pharmaceutical manufacturers to prove the safety of prescription drugs before marketing?
• What document or action is needed for transferring prescription information for refills?
• Which dosage form is MOST likely to present problems with bioequivalence?
• To be admitted to a comprehensive maintenance program, how long must narcotic-dependent individuals have been physiologically dependent on narcotics?
• The practice of pharmacy is considered to affect which aspects according to state regulations?
• For the NDC number 1074012804, what does 10740 represent?
• Is it mandatory for all oral dosage units to have an imprint according to regulations?
• What is a primary responsibility of a pharmacist concerning narcotic prescriptions?
• If a drug is found to have a new indication, which regulatory action should the manufacturer consider taking?
• Drug products with which of the following codes may be substituted for one another?
• What is required in patient package inserts for oral estrogen therapy?
• A medical food differs from food for special dietary use by requiring what?
• A drug product consisting of tablets may be declared misbranded under which guideline?
• When a patient begins a comprehensive narcotic treatment program, what must the first day's dose of methadone generally not exceed?
• A pharmacist with an inactive license for more than 5 years must complete which examinations to be relicensed?
• Which of the following is NOT acceptable regarding refills?
• The term "Grandfathered" in pharmaceuticals refers to drugs marketed before which act?
• What requirement applies to the name printed on a controlled substance prescription?
• Which act is the Consumer Product Safety Commission responsible for?
• Is USAN the final authority for new drug names?
• Can a Charitable Clinic Pharmacy only obtain drugs from an institutional facility for re-dispensing?
• Which government agency oversees the regulation of controlled substances?
• Orphan drugs are defined as drugs that are:
• Which law first required the statement "Caution: Federal law prohibits dispensing without a prescription" on drug product packaging?
• Which of the following is a Schedule II controlled substance?
• Which of the following drug products must be purchased using a DEA Form 222?
• What type of medication is a product containing 15 mg of hydrocodone per dose typically classified as?
• What is true regarding the sale of codeine-containing Schedule V cough medicine without a prescription?
• When taking an inventory of controlled substances, what is a necessary action?
• In the U.S., the name on the label of an herbal product must match which of the following reference sources?
• What type of product does the term 'over-the-counter' refer to?
• Which statement is NOT true regarding satellite clinics and keys?
• Conflicts between federal law and state law are resolved by recognizing that which law supersedes the other?
• Which drug requires a patient to sign an informed consent before receiving the original prescription?
• How long should unit dose drug packaging performed by a practitioner not exceed from the date of repackaging?
• What is the maximum distance a hospital pharmacy can compound drug products for healthcare facilities they own?
• Which form is used to order controlled substances, such as cocaine HCL?
• What terminology is used in the USP/NF classification system for home-use sterile drug products?
• True or False: CGMP applies only to sterile product manufacturing.
• True or False: Medical foods must always be prescribed before administration to patients.
• What must a pharmacy do when preparing a topical formula that contains a prescription drug?
• How can a physician obtain cocaine HCL powder for local anesthetic use?
• A cosmetic company markets an OTC topical cream claiming to reverse psoriatic lesions. Who may legally challenge this claim?
• What is the correct term for the document that contains formal charges against a pharmacy professional?
• What is the longest "beyond use" expiration date a pharmacist may place on a prescription labeled with an expiration date of 1/2017 if filled on 1/2/2014?
• Which type of warning is necessary for certain OTC products for the protection of nursing women?
• How are orphan drugs typically classified?
• How many hours of continuing pharmacy education must a Tennessee pharmacist complete for license renewal?
• The USP/NF is best described as a publication that is published by?
• Patients attempting to purchase drugs from online websites should look for which medallion on the site?
• What category does Methamphetamine fall under in drug classifications?
• What is the clinical trial phase number associated with post-marketing surveillance of a drug?
• What federal law was enacted in response to the meningitis outbreak tied to pharmacy compounding?
• What purpose does "Tall Man Lettering" serve in medication safety?
• A DEA Form 222a is used for what purpose?
• Which actions by a company offering Medicare Plan D coverage are NOT permitted?
• Which of the following substances is classified as a Schedule IV drug?
• What is the primary objective of individual state boards of pharmacy?
• Which phrase best describes the implications of the FDA regulations for pharmacy compounding?
• If an outsourcing facility compounds prescription drug products, how must these products be compounded?
• Which category of drugs requires a warning on prescription containers about transfers?
• What principle allows patients to participate in end-of-life decisions?
• What can an FDA inspector cite a community pharmacy for?
• A physician who is a resident in a hospital without a DEA registration number can prescribe controlled substances in which way?
• What is the federal act that restricts the re-importation of previously exported drugs?
• Which of the following individuals is exempt from registration under the Controlled Substance Act?
• Which of the following drug products is a controlled substance?
• Which FDA unit is responsible for overseeing prescription drug advertising?
• Which of the following are Schedule II controlled substances?
• A product with not more than 1.8 g of codeine per 100 mL is assigned to which Schedule?
• Is unit dose drug packaging subject to the same requirements as bulk drug packaging?
• A pharmaceutical manufacturer requesting patient information from a pharmacy for discount coupons likely violates which law?
• What is the purpose of a quality assurance program in pharmacy practice?
• Which portion of the federal counseling regulations must be performed by a committee appointed within each individual state?
• What does PDMA stand for?
• Narcotic drugs may be dispensed to treat narcotic dependence in which of the following facilities?
• What essential feature is required for a pharmacy to comply with HIPAA regulations?
• Which volume of the USP DI contains significant information about drug product bioequivalence?
• For a pharmacy to be eligible for exemptions under section 503A, which of the following must they do?
• Which medication used to treat narcotic dependence is available in a sublingual form?
• Which of the following is not a sponsor of USAN?
• Which category do all the following drugs belong to, except one?
• Which of the following correctly identifies a restriction of Schedule III substances?
• How long can the remaining portion of a partially filled Schedule II prescription be filled?
• What must a pharmacist ensure when dispensing codeine-containing medications?
• Which law regulates the confidentiality of patient health information in a pharmacy?
• Which of the following barbiturates is classified in controlled substances category IV?
• The Notice of Hearing and Charges will refer to you as the __________.
• What is required for compounding prescription drugs prior to receiving a prescription?
• In which location would you not find a pharmaceutical manufacturer's drug sample?
• Under which circumstances may Schedule II prescriptions be partially filled?
• Is the imprint requirement for solid oral dosage units applicable only to tablets?
• If the renewal fee is not paid, how many days before a health care provider's license is revoked?
• Which of the following notifications does not have specific HIPAA requirements?
• The caution statement regarding transferring prescribed drugs is *not* needed for which situation?
• When conducting a controlled substance inventory, which of the following must be included?
• Which of the following describes a scheduled drug?
• What should pharmacies do if any DEA Form 222 is lost?
• What must be true about prescriptions for isotretinoin?
• What must be documented when a prescription is returned to stock?
• According to federal guidelines, where should the pharmacist indicate the date on which a prescription refill is dispensed?
• What does the process of completing an internal incident report and taking corrective actions represent?
• An applicant for initial pharmacist licensure in Tennessee must show that they have completed a minimum of how many hours of pharmacy internship?
• Which of the following is NOT an acceptable means for obtaining prescription medications when the pharmacy site is closed?
• Which record system is primarily checked for a criminal background check during initial licensure?
• What does the abbreviation OTC stand for in pharmaceuticals?
• The expiration date on a commercial pharmaceutical product is July 2016. When will this product be considered expired?
• If a pharmaceutical company requests patient information regarding a certain antidepressant drug, what is the ethical concern?
• Which of the following drug products must be purchased by pharmacies using DEA Form 222?
• What must labels of nonprescription drug products for oral use indicate?
• Percogesic is classified as which of the following?
• Which factor contributes to the classification of a drug as an orphan drug?
• Which controlled substance may be partially filled upon patient request?
• Which information must be included in the bar code of drug products sold to hospitals?
• Which one of the following dosage forms is least likely to present bioequivalence problems?
• What adjuvant's presence in a drug product requires a special label warning?
• Which term describes using a system to ensure medication accuracy during dispensing?
• What are "grandfathered" drugs?
• Violating the Tennessee pharmacy practice Act is classified as which type of misdemeanor?
• What requirements must a prescription meet to be valid?
• For off-label therapeutic use of drugs, where can pharmacists find relevant information?
• Dronabinol is classified under which schedule of controlled substances?
• When refilling a prescription that requires a child-resistant container, the pharmacist must always replace which of the following?
• Which agency is responsible for regulating the safety of dietary supplements?
• What must be ordered from a wholesaler using DEA order form 222?
• What drug is the iPLEDGE program designed to ensure safe dispensing for?
• Which protocol must a hospital pharmacy follow to possess pharmaceutical manufacturer's drug samples?
• Under which condition can practitioners of Traditional Chinese Medicine sell ephedra-containing products?
• A statutory section in the Tennessee Pharmacy Practice Act conflicts with a Tennessee Board of Pharmacy Rule. Which is the controlling law?
• What is an acceptable usage for cranberry extract as per herbal regulations?
• What is the threshold percentage of out-of-state prescriptions a pharmacy can send before being cited by the FDA?
• What is the primary role of the FDA regarding drugs used in veterinary practices?
• Under what circumstance can Ipecac Syrup be sold without a prescription?
• Which body oversees the selection of nonproprietary names for new drugs?
• Under which of the following situations would a drug product be considered misbranded?
• Which dosage forms of secobarbital must be ordered using a DEA Form 222?
• Sponsors of Medicare Plan D programs must provide a broad choice of formulary drugs for each of the following drug categories except:
• What must an outsourcing facility allow the FDA to do?
• Ephedra is no longer allowed in which type of product in community pharmacies?
• A client requests a refill on a prescription for Diphenhydramine 25 mg with a Sig reading "one cap 1h before bedtime and 1 hs if needed". What is the most appropriate action for the pharmacist?
• Which of the following can a certified pharmacy technician NOT perform?
• Which of the following statements is true about controlled substance prescriptions?
• What permanent identification must a pharmacy possess to electronically bill Medicare or Medicaid for prescriptions?
• DEA registration numbers for mid-level practitioners generally begin with which letter?
• The number of pharmacy technicians can be increased to what maximum, based on public safety considerations?
• What must be considered when purchasing a large supply of medication?
• According to federal law, which schedules of controlled substances can be dispersed throughout a community pharmacy's stock?
• In the National Drug Code (NDC), what does the first series of digits represent?
• What designation indicates that drug products of the same strength and dosage form may be considered interchangeable?
• What must a hospital do with taxes-exempt grain alcohol at the end of the year?
• What must prescribers do for all controlled substances administered during narcotic detoxification treatment?
• Which product listed would be classified as a Schedule III controlled substance?
• When conducting a controlled substance inventory, how must Schedule II substances be counted?
• What is the purpose of prescribing methadone by a physician at a narcotic treatment facility?
• Which statement correctly reflects the role of the FDA regarding drug names?
• Which of the following is *not* considered a controlled substance?
• Which information is not required on the labeling of a prescription container for Schedule III controlled substances?
• Which component is a generic term designating drugs that can be marketed under their nonproprietary name?
• Which of the following statements is NOT true regarding electronic prescribing of controlled substances?
• What is true about DEA Form 222?
• Which of the following must be barcoded in a hospital pharmacy?
• What is the total number of digits allowed in the NDC numbers on a pharmaceutical package?
• Eszopiclone is an example of a drug product in which controlled substance schedule?
• What is the maximum number of pharmacy technicians allowed per pharmacist on a typical day?
• The advertising to the general public of OTC drugs is basically under the regulatory responsibilities of which agency?
• Which of the following is a Schedule IV controlled substance?
• Which of the following is considered a Schedule I controlled substance?
• What acronym does the USP use for sterile products prepared for home delivery?
• What type of substance is methadone classified as?
• In what situation can a pharmacist accept oral orders for Schedule II drugs?
• If a new drug product is named "felorazepam", what is its likely classification?
• Which drug is considered to be a "Basic Class" drug under the Controlled Substances Act?
• Which of the following substances is classified as a Schedule I drug?
• Which organization is responsible for accrediting health institutions such as hospitals?
• The USAN designates which of the following?
• Which of the following drugs is a common treatment option for narcotic dependence?
• Who is allowed to compound a prescription drug product under section 503A?
• How must ingredients be listed on cosmetic package labels?
• What must be done to Schedule IV substances in opened containers during an inventory?
• What is required of pharmacies when handling controlled substances?
• Which organization is primarily responsible for evaluating the safety and effectiveness of drugs used in veterinary practices?
• Which action is legal for a pharmacist if a patient has not picked up their prescription?
• Which organization is primarily responsible for overseeing Medicare programs?
• Which phase in drug development is characterized by postmarketing studies?
• Which of the following is a requirement for an outsourcing facility registered with the FDA?
• What is the major objective of the Electronic Orange Book?
• Where can a statement about a specific OTC product having a tamper-evident feature NOT be placed?
• Which of the following best describes a controlled substance?
• What is one major objective for developing a formulary?
• What is the primary purpose of labeling medications with the caution statement about patient transfer?
• Which statement regarding electronic prescribing is accurate?
• Which amendment was the first to require that pharmaceutical manufacturers prove the efficacy of prescription drugs before marketing?
• Which one of the following actions is permissible in a hospital that has tax-free alcohol?
• The statement ''Rx only'' does NOT need to appear on the packaging of?
• What is required for each partial filling of a Schedule IV controlled substance?
• What action should a pharmacist take if a patient refuses to be counseled about a new prescription?
• Under what condition can a pharmacy dispense compounded psoriasis cream for patients of other prescribers?
• In reference to controlled substances, what does the AB code indicate?
• Which task can a technician perform regarding oral medical and prescription orders?
• What is permissible for any physician concerning narcotic withdrawal symptoms?
• A patient has a prescription for a controlled substance that has expired. What is the pharmacist's next step?
• A product that contains 60 mg of codeine and 325 mg of acetaminophen is most likely classified as:
• Which drug has a similar regulatory status as Zolpidem?
• Under what circumstance might a pharmacy be considered to be manufacturing?
• Which statement regarding DEA Form 222 is accurate?
• Who must be registered with the DEA to dispense controlled substances in a hospital pharmacy?
• Under what circumstance can samples of prescription drugs be given to patients?
• What should a technician do before administering medications to a patient?
• What is the maximum grams of methamphetamine precursor a pharmacy may sell in 30 days?
• What does “adequate directions for use” mean for over-the-counter drugs?
• According to federal regulations, which dosage form is prohibited from having color additives?
• In regards to hormonal contraceptives, can pharmacists provide them under a collaborative practice agreement to individuals under 18 years of age?
• Hospitals intending to use significant amounts of tax-free grain alcohol should acquire which form?
• What’s the primary purpose of the Drug Price Competition and Patent Term Restoration Act?
• The Rx department in a retail pharmacy must occupy a space of not less than how many square feet?
• Which of the following is used in the treatment of narcotic dependence?
• To be eligible for appointment to the pharmacy board, a consumer must be a resident of Tennessee for how many years?
• Which drug is commonly used for the treatment of opioid addiction?
• Excipients in pharmaceutical dosage forms are typically found on which list?
• Which statements regarding drug recalls are accurate?
• Which acronym is most associated with health care reimbursement?
• Which type of employee is authorized to administer or dispense drugs in a narcotic treatment program?
• For which of the following must oral administration drug products have an identifying imprint?
• Which category of drugs requires the label "Rx only" to be present on the manufacturer's package?
• When a customer requests quinine 260 mg tablets, which of the following responses is appropriate?
• Which of the following statements about recalled prescription drugs in a pharmacy is correct?
• Under what condition may a pharmacist partially fill a Schedule II prescription?
• Which drug requires a patient to sign an informed consent prior to receiving an original prescription?
• Which statement about the National Drug Code (NDC) is true?
• Which component is commonly included in controlled substance inventories?
• Which of the following is not a requirement for labeling prescription drugs?
• What is required of practitioners who prescribe controlled substances electronically?
• Which of the following is true of DEA Form 222?
• What is the maximum pharmacist to pharmacy technician ratio without special considerations?
• What specific requirement does the label of an OTC bottle of Ipecac Syrup have?
• Oral authorization for additional refills on a Schedule III prescription is acceptable under which condition?
• Which of the following actions is acceptable for a prescriber regarding refills on Schedule III prescriptions?
• For which situation is it permissible to fax a prescription for Schedule II drugs?
• What type of medication is considered ineffective for treating nocturnal leg cramps in over-the-counter formulations?
• A pharmacy chain with multiple locations must obtain what for each individual pharmacy?
• Which item is not required on the label of a parenteral product?
• What must be done if a prescription label indicates an expiration date?
• True or False: A pharmacist with an inactive license for more than 5 years is required to take both the NAPLEX and MPJE to relicense.
• Which of the following would be considered as an incidence of misbranding?
• A pharmacist may refuse to accept or fill a prescription under all of the following circumstances EXCEPT when:
• What must labels of commercial drug products intended for electrolyte replacement express concentration in?
• What must be included on a pharmaceutical product label according to regulatory guidelines?
• How long must records for controlled substances be kept?
• Which of the following products are considered Schedule III controlled substances?
• What type of products must comply with the requirements set by the Poison Prevention Packaging Act?
• A filled DEA Form 222 must be kept by the:
• For Schedule IV controlled substances, what is required for partial fillings?
• What is required for the proper storage of controlled substances?
• Which statement on a cranberry extract label would be compliant with DSHEA regulations?
• Which of the following is permissible when taking a controlled substance inventory?
• If a pharmaceutical company's tablets fail to meet the expected expiration dating, the lot may be considered:
• What is the maximum number of refills allowed for a Schedule III prescription within a six-month period?
• What is required for a physician to dispense narcotic treatment for dependence?
• What is a legal way for a pharmacist to contact a patient about a prescription?
• How frequently must a pharmacy have a patient sign a new notice of privacy practices under HIPAA?
• What is a permissible use of tax-free alcohol purchased by a hospital?
• What is the maximum duration for short-term narcotic detoxification treatment?
• The statement "The practice of pharmacy within the state is declared to be... subject to regulation" is based on what concept?
• Which entity is primarily responsible for enforcing the Federal Food, Drug, and Cosmetic Act?
• What label claim can an herbal product like Saw Palmetto make under the present DSHEA?
• Under which condition would a drug product be considered adulterated?
• True or False: Conflicts between federal law and state law are resolved by federal law superseding state law.
• Which action is permissible under FDA rules for prescription compounding by pharmacies?
• What should a pharmacist do immediately upon discovering a dispensing error?
• According to federal law, what must be included on a prescription label?
• What is the maximum volume of Ipecac Syrup that can be sold without a prescription?
• What is the minimum requirement for continuing education hours during a two-year licensure renewal cycle in Tennessee?
• Which drug product is not classified as a controlled substance?
• Which of the following is a primary purpose of a formulary?
• A community pharmacy preparing 5,000 sustained-release capsules may be cited for which reason?
• Which of the following statements is false regarding filling prescriptions for controlled substances?
• Which of the following best defines a "controlled substance"?
• How long should a practitioner keep records of repackaged medication?
• Which controlled drugs may a pharmacist mail through the US Postal Service?
• Which piece of information is not part of a drug product's National Drug Code (NDC)?
• Which method allows for the issuance of Schedule III, IV, and V controlled substance prescriptions to a community pharmacy?
• The acronym DUR is most closely associated with which aspect of pharmacy practice?
• What is the term used in HIPAA privacy rules for removing patient identifying information during discussions?
• If authorization is not obtained within the first 72-hour supply, how many additional days are allowed to dispense?
• Which category of standards does the Electronic Orange Book classify prescription medications under?
• What should a pharmacy do if it needs to return Schedule II drugs?
• How many 30 mg Sudafed tablets can a 35-year-old customer purchase at one time?
• The classification of drugs into controlled substance schedules by the federal government is primarily based on what factor?
• If a marketed drug product has a new use for another condition, what must the manufacturer do to claim this indication?
• The drug price competition and Patent Term Restoration Act provides how many additional years of patent protection?
• What is the primary function of Medicaid?
• For ratio purposes, how are interns classified?
• What is an example of a drug that is used in combination with methadone for treating opioid dependence?
• What is an acceptable action for a pharmacy when a physician shares a topical moisturizing formula containing a prescription drug?
• What is the time frame in which a change of licensure address must be reported?
• Under what condition is a faxed Schedule II prescription permitted from a prescriber to a pharmacy?
• When counseling a customer about a body lotion that does not contain tartrazine, the pharmacist should explain that:
• An orphan drug is characterized by which of the following?
• What does postmarketing surveillance of a drug product refer to?
• When explaining the Medicare Plan D program, which detail should a pharmacist emphasize to a couple?
• What must a community pharmacy track when handling controlled substances?
• How many square feet must the Rx department occupy in a retail pharmacy?
• What type of information is useful but not mandatory on OTC product labels?
• In what scenario can a pharmacist fill a prescription without complete medical history?
• Which form is used to apply for a new DEA registration for a community pharmacy?
• For which reason can a drug product consisting of tablets be declared adulterated?
• A package for nonprescription products designed to prevent the addition of foreign material is best described as being?
• What is the primary purpose of a drug utilization review (DUR)?
• True or False: A medical food is intended for use under medical management.
• In what situation can a pharmacist legally discuss a prescription with a patient?
• How would the Electronic Orange Book categorize a new drug entity first placed on the market by a company?
• How often do sterile products need to be reported?
• What is required for a prescription for a controlled substance to be valid?
• Which of the following statements is correct about controlled substances?
• Which part of the pharmacy intern's responsibilities can they take on with direct supervision?
• What may the hospital pharmacy director issue if an employee is charged with a drug offense?
• What is the key feature of a peer review program in pharmacy?
• What is the most important factor in determining whether a community pharmacy must comply with HIPAA regulations?
• Which of the following statements is true regarding office use prescriptions under section 503A?
• If a patient refuses to provide medical information for a prescription profile, what can the pharmacist do?
• Who is a primary group covered under the Medicare Modernization Act of 2003?
• Which of the following is NOT a part of the Prescription Drug Marketing Act of 1987 (PDMA)?
• What is the therapeutic classification of the 'date-rape drug'?
• What is the authorized penalty for each violation in the context provided?
• Which of the following is a characteristic of narrow therapeutic index drugs?
• Which of the following is true about Medicare Plan D?
• Therapeutic substitution is allowed only if an institution is?
• Which prescription action is not allowed under narcotic treatment facility regulations?
• Which of the following is a requirement for solid oral dosage forms regarding imprinting?
• What is one requirement for therapeutic substitution in healthcare institutions?
• A new cough syrup contains 15 mg of codeine phosphate and 100 mg of guaifenesin in each 10 mL dose. What would this product likely be classified as?
• Can a practitioner issue a prescription for "office use" according to section 503A?
• Pharmacists are required to periodically inventory supplies of which type of drug product?
• Which ingredients must be included on pharmaceutical product labels?
• What other type of drug is excluded from the "Grand-fathered Drugs" category?
• Which congressional action included the requirement for pharmacists to counsel patients about their prescriptions?
• Which of the following products are exempt from FDA regulations concerning expiration dating?
• Which statement regarding barcoding of prescription drug labels is accurate?
• Which of the following active ingredients is typically regulated under controlled substances?
• What is designated for every new drug placed on the market?
• Which designation has replaced the statement "Caution: Federal law prohibits dispensing without a prescription" for drug products that require a prescription in the United States?
• Prior to selling a compounded drug product, what must a pharmacy do according to section 503A?
• What is the time interval for newly eligible individuals to enroll in Medicare Plan D without incurring a penalty?
• What is true about DEA Form 222 regarding unfilled orders?
• What action may a hospital pharmacy director take if an employee is convicted of selling drugs according to the Federal Anti-Drug Abuse Act 1988?
• Which item is NOT considered a controlled substance?
• What function can a pharmacy intern perform under direct pharmacist supervision?
• In an ambulatory care comprehensive narcotic treatment program, by which route may patients receive methadone doses?
• Under section 503A of the federal Food, Drug and Cosmetic Act, what should pharmacies maintain records of?
• Is Cocaine considered a narcotic substance?
• Who ultimately retains Copy 3 of DEA Form 222?
• What is the purpose of risk evaluation and mitigation strategies (REMS)?
• What action must an outsourcing facility take regarding safety events associated with their compounded drug products?
• A pharmacist may issue a Power of Attorney to allow an individual to:
• What type of prescription may be transferred on a one-time basis for dispensing a refill?
• Controlled substance inventories must be made for which of the following?
• Who is authorized to designate the "official" name for a new drug?
• Which statement is true regarding the dispensing of controlled substances?
• Which of the following drug products is exempt from the Poison Prevention Packaging Act?
• Which label information is NOT required on the unit dose packages prepared in a hospital?
• Phenobarbital is classified as which type of controlled substance?
• Pseudoephedrine is classified as which of the following?
• What is the term for using an FDA approved drug for a purpose not officially approved?
• What is commonly detected through blood and urine tests in narcotic maintenance treatment programs?
• Which form is required in order for a pharmacy to purchase Schedule I or II controlled substances?
• Which statement regarding prescribers and controlled substances is true?
• What is a requirement for a schedule II controlled substance prescription according to the law?
• What is one primary characteristic of Schedule II controlled substances?
• What is the maximum percentage of remaining time allowed when performing unit dose drug packaging?
• Which regulatory body is responsible for overseeing the efficacy and safety of pharmaceuticals?