KANSAS MPJE PACKAGED FINAL TEST
2026 QUESTIONS WITH CORRECT ANSWERS
GRADED A+
• What must be provided with the ANDA.
Answer: Proof that the new drug has the same active ingredient, ROA,
dosage from, strength, and its bioequivalent
• performed by DUR board of physicians and pharmacist to review
medication use trends and data over a specified period of time and attempt
to evaluate and improve medication use.
Answer: Retrospective Drug Use review
• 2.
Answer: Number of years a vaccination protocol that establishes what
vaccines a pharmacist may administer, procedures for record keeping, and
emergency response is considered valid
• Medicare Part B.
Answer: The part of the Medicare program that pays for physician services,
outpatient hospital services, durable medical equipment, and other services
and supplies.
• Combat Meth Act 2005.
Answer: Place ephedrine, pseudoephedrine and phenylpropanolamine in the
"Scheduled Listed Chemcial products". May not sell such products in
nonliquid form at retail unless the product is blister packs. (Max 2 dosage
units in each blister).
• approved drug products with therapeutic equivalence evaluations.
Answer: Orange Book
• Federal offense to tamper with consumer products Requires tamper resistant
packaging for OTC.
, Answer: Federal Anti-Tampering Act of 1982
• If a pharmacist is a PIC, what is the special requirement they need to do?.
Answer: They must have a score of at least 85% on a law exam that include
statutes, rules, and regulations of both state and federal pharmacy laws.
• 3.6.
Answer: Number of grams maximum of pseudoephedrine base that may be
sold to a single patient in a day
• Can a controlled substance be issued with out an in-person evaluation via an
online pharmacy?.
Answer: NO it violates the CSA and is against DEA rule
• one that supports or sustains human life or is of substantial importance in
preventing impairment of human health or presents a potential, unreasonable
risk of illness or injury.
Answer: Class 3 Medical Device
• Codeine guidelines for C3 status.
Answer: NOT FOR KIDS 1.8g codeine/100mL 90mg/dose
• Does Kansas adhere to USP For compounding?.
Answer: No they have their own act (Chemical Control Act and Uniform
Controlled Substances Act)
• Does Kansas allow prescriptions from out of state prescribes?.
Answer: yes
• DEA form 224/224a/225b.
Answer: 224: initial registration as DISPENSER 224a: Renewal registration
form as DISPENSER 224b: Chain dispenser MUST BE DONE EVERY 3
YEARS
• Form 41.
Answer: Form to request permission to destroy damaged, outdated, or
unwanted controlled substances
• How are OTC drugs approved by the FDA? (2 ways).
, Answer: Either NDA process or OTC monograph
• Magnesium max before warning must be given.
Answer: 975mg
• Does Kansas issue temporary licenses?.
Answer: no
• Form 224.
Answer: Form used to apply for a new DEA dispenser registration
• Classification of all devices into 3 classes based on the degree of control
necessary to assue safety and effectiveness; most regulated are class 3.
Answer: Medical Device Amendment of 1976
• What can the DEA not inspect?.
Answer: Financial, Sales, and Pricing Data
• What must be in place for immunizations?.
Answer: A vaccination protocol
• Form 363.
Answer: Form used to apply for a new DEA narcotic treatment program
registration
• Form 106.
Answer: Form to report substantial theft or loss of controlled stubstances
• What is a DATA waived physician?.
Answer: One who has been trained to treat addiction
• Does Kansas require interns to be licensed or registered? If so how long
does the registartion last?.
Answer: yes. last 6 years
• C3 morphiene guideline.
Answer: 50mg morphiene/100mL or 100g w/another drug
• "Adequate information for use".
Answer: Labeling requirements for Rx Drugs
2026 QUESTIONS WITH CORRECT ANSWERS
GRADED A+
• What must be provided with the ANDA.
Answer: Proof that the new drug has the same active ingredient, ROA,
dosage from, strength, and its bioequivalent
• performed by DUR board of physicians and pharmacist to review
medication use trends and data over a specified period of time and attempt
to evaluate and improve medication use.
Answer: Retrospective Drug Use review
• 2.
Answer: Number of years a vaccination protocol that establishes what
vaccines a pharmacist may administer, procedures for record keeping, and
emergency response is considered valid
• Medicare Part B.
Answer: The part of the Medicare program that pays for physician services,
outpatient hospital services, durable medical equipment, and other services
and supplies.
• Combat Meth Act 2005.
Answer: Place ephedrine, pseudoephedrine and phenylpropanolamine in the
"Scheduled Listed Chemcial products". May not sell such products in
nonliquid form at retail unless the product is blister packs. (Max 2 dosage
units in each blister).
• approved drug products with therapeutic equivalence evaluations.
Answer: Orange Book
• Federal offense to tamper with consumer products Requires tamper resistant
packaging for OTC.
, Answer: Federal Anti-Tampering Act of 1982
• If a pharmacist is a PIC, what is the special requirement they need to do?.
Answer: They must have a score of at least 85% on a law exam that include
statutes, rules, and regulations of both state and federal pharmacy laws.
• 3.6.
Answer: Number of grams maximum of pseudoephedrine base that may be
sold to a single patient in a day
• Can a controlled substance be issued with out an in-person evaluation via an
online pharmacy?.
Answer: NO it violates the CSA and is against DEA rule
• one that supports or sustains human life or is of substantial importance in
preventing impairment of human health or presents a potential, unreasonable
risk of illness or injury.
Answer: Class 3 Medical Device
• Codeine guidelines for C3 status.
Answer: NOT FOR KIDS 1.8g codeine/100mL 90mg/dose
• Does Kansas adhere to USP For compounding?.
Answer: No they have their own act (Chemical Control Act and Uniform
Controlled Substances Act)
• Does Kansas allow prescriptions from out of state prescribes?.
Answer: yes
• DEA form 224/224a/225b.
Answer: 224: initial registration as DISPENSER 224a: Renewal registration
form as DISPENSER 224b: Chain dispenser MUST BE DONE EVERY 3
YEARS
• Form 41.
Answer: Form to request permission to destroy damaged, outdated, or
unwanted controlled substances
• How are OTC drugs approved by the FDA? (2 ways).
, Answer: Either NDA process or OTC monograph
• Magnesium max before warning must be given.
Answer: 975mg
• Does Kansas issue temporary licenses?.
Answer: no
• Form 224.
Answer: Form used to apply for a new DEA dispenser registration
• Classification of all devices into 3 classes based on the degree of control
necessary to assue safety and effectiveness; most regulated are class 3.
Answer: Medical Device Amendment of 1976
• What can the DEA not inspect?.
Answer: Financial, Sales, and Pricing Data
• What must be in place for immunizations?.
Answer: A vaccination protocol
• Form 363.
Answer: Form used to apply for a new DEA narcotic treatment program
registration
• Form 106.
Answer: Form to report substantial theft or loss of controlled stubstances
• What is a DATA waived physician?.
Answer: One who has been trained to treat addiction
• Does Kansas require interns to be licensed or registered? If so how long
does the registartion last?.
Answer: yes. last 6 years
• C3 morphiene guideline.
Answer: 50mg morphiene/100mL or 100g w/another drug
• "Adequate information for use".
Answer: Labeling requirements for Rx Drugs
