KANSAS MPJE PACKAGED PRACTICE
EXAMINATION 2026 QUESTIONS WITH
ANSWERS GRADED A+
• Xyrem.
Answer: Sodium Oxybate CIII
• TussiCaps.
Answer: Chlorpheniramine/Hydrocodone C-II
• Law that contained the Compounding Quality Act that distinguishes 503A
and 503B facilities as well as the Drug Supply Chain Security Act to track
and trace the chain.
Answer: Drug Quality and Security Act (DQSA) of 2013
• Compounded in an ISO 5 PEC in a cleanroom with additional requirements
(stability/sterility testing) category?.
Answer: Category 3
• Is there a quantity limit on CII prescriptions?.
Answer: No
• Established a distinction between OTC and Rx products. Rx products were
called "Legend Drugs".
Answer: Durham-Humphrey Amendment of 1951
• Amended the FDCA to required drugs to have NDC numbers.
Answer: Drug Listing Act of 1972
• What unique signature requirements exist for faxed prescriptions?.
Answer: Must be a manual signature
• A pharmacy tech must notify the board within 30 days of....
Answer: 1) name change 2) change of email 3) change of address 4) change
of employer 5) quitting
,• A C-II without a prescriber signature.
Answer: Return to patient to have prescriber fix
• Under federal law, DEA Form 222s must be kept for.
Answer: 2 years
• Prescription hard copy storage regulations.
Answer: Must be retained for 5 years; must be "Readily retrievable" means
that records kept in hard copy or by automatic data processing applications
or other electronic or mechanized record-keeping systems can be separated
out from all other records quickly and easily during an inspection or
investigation, or within a reasonable time not to exceed 48 hours of a written
request from the Board or other authorized agent.
• Minimum intern hours.
Answer: 1740
• Which pseudoephedrine sale does NOT require documentation in a
logbook?.
Answer: A single dose (1 or 2 30 mg tablets)
• How much can an optometrist dispense?.
Answer: 24 hours worth or minimum quantity until prescription can be filled
by a pharmacist
• Application for New Facility Registration for dispensing Controlled
Substances.
Answer: DEA Form 224
• Where must vaccine records be kept? How long?.
Answer: At the pharmacy, even if administered offsite. 5 years.
• How often are CQI meetings held?.
Answer: Every 90 days
• Can a pharmacist fill a prescription from Canada?.
Answer: No. Must be in the US or a US territory
• What form is used to report loss or theft of a control substance?.
, Answer: DEA form 106
• Under federal law, CS records must be kept for.
Answer: 2 years
• Required manufactures to not just prove safety (FDCA of 1938) but also
efficacy , as well as serious side effects, informed consent, and the FDA
conducted retrospective drug efficacy investigations through the DESI
program.
Answer: Kefauver-Harris Amendment of 1962
• Can a control substance be prescribed for treatment of weight loss?.
Answer: Only 30 day supplies at a time may be written if a control
substance (phentermine, qsymia). Amphetamines cannot be written for
weight loss.
• What restriction does the Prescription Drug Marketing Act of 1987 place on
hospitals regarding drug purchases?.
Answer: It blocks hospitals from reselling drugs they purchased at a
discount.
• Established regulations for dietary supplements and did not need FDA
approval prior to marketing.
Answer: Dietary Supplement Health and Education Act (DSHEA) of 1994
• Can pharmacy containers be reused?.
Answer: No Prohibited under PPPA of 1970
• To use an interchangeable biosimilar, what must a pharmacist do?.
Answer: Inform the patient and communicate to the prescriber within 5
business days
• In issuing multiple CII prescriptions, how many days can me prescribed?.
Answer: 90 total days among prescriptions
• Drugs that are filthy, putrid, prepared in unsanitary conditions,
contaminated, lower purity/quality than official standards, or not listed in
official compendia are classified as _____.
EXAMINATION 2026 QUESTIONS WITH
ANSWERS GRADED A+
• Xyrem.
Answer: Sodium Oxybate CIII
• TussiCaps.
Answer: Chlorpheniramine/Hydrocodone C-II
• Law that contained the Compounding Quality Act that distinguishes 503A
and 503B facilities as well as the Drug Supply Chain Security Act to track
and trace the chain.
Answer: Drug Quality and Security Act (DQSA) of 2013
• Compounded in an ISO 5 PEC in a cleanroom with additional requirements
(stability/sterility testing) category?.
Answer: Category 3
• Is there a quantity limit on CII prescriptions?.
Answer: No
• Established a distinction between OTC and Rx products. Rx products were
called "Legend Drugs".
Answer: Durham-Humphrey Amendment of 1951
• Amended the FDCA to required drugs to have NDC numbers.
Answer: Drug Listing Act of 1972
• What unique signature requirements exist for faxed prescriptions?.
Answer: Must be a manual signature
• A pharmacy tech must notify the board within 30 days of....
Answer: 1) name change 2) change of email 3) change of address 4) change
of employer 5) quitting
,• A C-II without a prescriber signature.
Answer: Return to patient to have prescriber fix
• Under federal law, DEA Form 222s must be kept for.
Answer: 2 years
• Prescription hard copy storage regulations.
Answer: Must be retained for 5 years; must be "Readily retrievable" means
that records kept in hard copy or by automatic data processing applications
or other electronic or mechanized record-keeping systems can be separated
out from all other records quickly and easily during an inspection or
investigation, or within a reasonable time not to exceed 48 hours of a written
request from the Board or other authorized agent.
• Minimum intern hours.
Answer: 1740
• Which pseudoephedrine sale does NOT require documentation in a
logbook?.
Answer: A single dose (1 or 2 30 mg tablets)
• How much can an optometrist dispense?.
Answer: 24 hours worth or minimum quantity until prescription can be filled
by a pharmacist
• Application for New Facility Registration for dispensing Controlled
Substances.
Answer: DEA Form 224
• Where must vaccine records be kept? How long?.
Answer: At the pharmacy, even if administered offsite. 5 years.
• How often are CQI meetings held?.
Answer: Every 90 days
• Can a pharmacist fill a prescription from Canada?.
Answer: No. Must be in the US or a US territory
• What form is used to report loss or theft of a control substance?.
, Answer: DEA form 106
• Under federal law, CS records must be kept for.
Answer: 2 years
• Required manufactures to not just prove safety (FDCA of 1938) but also
efficacy , as well as serious side effects, informed consent, and the FDA
conducted retrospective drug efficacy investigations through the DESI
program.
Answer: Kefauver-Harris Amendment of 1962
• Can a control substance be prescribed for treatment of weight loss?.
Answer: Only 30 day supplies at a time may be written if a control
substance (phentermine, qsymia). Amphetamines cannot be written for
weight loss.
• What restriction does the Prescription Drug Marketing Act of 1987 place on
hospitals regarding drug purchases?.
Answer: It blocks hospitals from reselling drugs they purchased at a
discount.
• Established regulations for dietary supplements and did not need FDA
approval prior to marketing.
Answer: Dietary Supplement Health and Education Act (DSHEA) of 1994
• Can pharmacy containers be reused?.
Answer: No Prohibited under PPPA of 1970
• To use an interchangeable biosimilar, what must a pharmacist do?.
Answer: Inform the patient and communicate to the prescriber within 5
business days
• In issuing multiple CII prescriptions, how many days can me prescribed?.
Answer: 90 total days among prescriptions
• Drugs that are filthy, putrid, prepared in unsanitary conditions,
contaminated, lower purity/quality than official standards, or not listed in
official compendia are classified as _____.
