Federal MPJE Practice Questions and answers
2025\2026 A+ Grade
what law prohibits the distribution of food and drugs that are misbranded or adulterated?
- correct answer Pure Food and Drug Act
What is the system that can be used as an electronic substitute for DEA Form 222 when ordering
Schedule II controlled substances?
- correct answer Controlled Substance Ordering System (CSOS)
What agency is responsible for the federal Controlled Substances Act (CSA)?
- correct answer the DEA
A pharmacist wants to know if generic warfarin tablets are bioequivalent to brand name Coumadin
tablets. Where can this information be found?
- correct answer The Orange Book
When a pharmacy submits a DEA Form 222 (single sheet) to purchase Schedule II controlled substances,
who keeps the original copy of the DEA Form 222?
- correct answer the supplier
Which DEA form must be completed and submitted to the DEA upon discovering a theft or significant
loss of controlled substances?
- correct answer DEA Form 106
What is the first application that must be submitted to the FDA before a drug can be administered to
humans in order to start testing?
- correct answer Investigational New Drug Application (IND)
Which phase of a clinical trial is first used to determine the efficacy of a drug?
- correct answer Phase II
, What Act regulates the sale and recordkeeping requirements for prescription drug samples?
- correct answer Prescription Drug Marketing Act
A manufacturer has a drug that is currently on the market, but they want to change the way the drug is
produced. What type of application must be submitted to the FDA in order to request approval for this
change?
- correct answer Prior Approval Supplement (PAS)
Which FDA expedited review program is intended for drugs that treat serious conditions and fill an
unmet medical need?
- correct answer Fast track
Schedule II controlled substances CANNOT be transferred in which of the following scenarios?
- correct answer A researcher would like to transfer excess Schedule II controlled substances to a
pharmacy to be dispensed to patients
A patient wants to refill a prescription but was not satisfied with the pharmacy that filled and dispensed
the prescription the first time. The patient demands the prescription be returned so they can take it to a
different pharmacy to obtain refills. The pharmacist should:
- correct answer offer to give a copy of the prescription to the patient, keep the original copy at the
pharmacy, and recommend the patient request the prescription be transferred to another pharmacy if
legal
An example of an adulterated drug is:
- correct answer a medication that has an unapproved color additive
What was the first law requiring drugs to be proven safe before being marketed?
- correct answer Food, Drug, and Cosmetic Act
What set of regulations specifies the required minimum manufacturing standards for pharmaceutical
products in the US?
- correct answer Good Manufacturing Practice (GMP)
2025\2026 A+ Grade
what law prohibits the distribution of food and drugs that are misbranded or adulterated?
- correct answer Pure Food and Drug Act
What is the system that can be used as an electronic substitute for DEA Form 222 when ordering
Schedule II controlled substances?
- correct answer Controlled Substance Ordering System (CSOS)
What agency is responsible for the federal Controlled Substances Act (CSA)?
- correct answer the DEA
A pharmacist wants to know if generic warfarin tablets are bioequivalent to brand name Coumadin
tablets. Where can this information be found?
- correct answer The Orange Book
When a pharmacy submits a DEA Form 222 (single sheet) to purchase Schedule II controlled substances,
who keeps the original copy of the DEA Form 222?
- correct answer the supplier
Which DEA form must be completed and submitted to the DEA upon discovering a theft or significant
loss of controlled substances?
- correct answer DEA Form 106
What is the first application that must be submitted to the FDA before a drug can be administered to
humans in order to start testing?
- correct answer Investigational New Drug Application (IND)
Which phase of a clinical trial is first used to determine the efficacy of a drug?
- correct answer Phase II
, What Act regulates the sale and recordkeeping requirements for prescription drug samples?
- correct answer Prescription Drug Marketing Act
A manufacturer has a drug that is currently on the market, but they want to change the way the drug is
produced. What type of application must be submitted to the FDA in order to request approval for this
change?
- correct answer Prior Approval Supplement (PAS)
Which FDA expedited review program is intended for drugs that treat serious conditions and fill an
unmet medical need?
- correct answer Fast track
Schedule II controlled substances CANNOT be transferred in which of the following scenarios?
- correct answer A researcher would like to transfer excess Schedule II controlled substances to a
pharmacy to be dispensed to patients
A patient wants to refill a prescription but was not satisfied with the pharmacy that filled and dispensed
the prescription the first time. The patient demands the prescription be returned so they can take it to a
different pharmacy to obtain refills. The pharmacist should:
- correct answer offer to give a copy of the prescription to the patient, keep the original copy at the
pharmacy, and recommend the patient request the prescription be transferred to another pharmacy if
legal
An example of an adulterated drug is:
- correct answer a medication that has an unapproved color additive
What was the first law requiring drugs to be proven safe before being marketed?
- correct answer Food, Drug, and Cosmetic Act
What set of regulations specifies the required minimum manufacturing standards for pharmaceutical
products in the US?
- correct answer Good Manufacturing Practice (GMP)
