FPGEE MANAGEMENT EXAM QUESTIONS AND
VERIFIED CORRECT ANSWERS LATEST 2026-2027
NEW VERSION
A hospital pharmacy is not required to first receive a patient-specific prescription or
order provided that the compounded drug products are only to healthcare facilities
that are owned and controlled the same entity that owns and controls the hospital
pharmacy and that are located within a *............* radius of the compounding
pharmacy - answer>>>*a. 1*
b. 3
c. 10
d. 12
An outsourcing facing that is registered with the FDA and subject to federal oversight
must comply with which of the following requirements (select all that apply: there is
more than one correct answer choice but not all answers choices are correct) -
answer>>>a. *Follow current good manufacturing practices (CGMP)*.
b. *Report adverse events. associated with the compounded drug product.*
c. *Allow FDA access to conduct inspections according to a risk-based schedule*.
d. Receive a prescription from a licensed practitioner prior to selling the
compounded drug
product.
e. Charge no more than the wholesale price of the least expensive commercial
available product currently being marketed in the United States
[True/false] Under section 503A of the federal Food, Drug and Cosmetic Act, a
pharmacy compounding prescription drug products should maintain records of any
calculations performed to determine the limited quantities of drug products
compounded before receipt of a prescription. - answer>>>*True*
, -
The name of the federal law enacted in 2013 in response to an outbreak of
meningitis due to
contamination of pharmacy compounding sterile products is the _____. -
answer>>>a. *Drug Quality and Security Act*
b. Pharmacy Compounding Safety Act
c. Compounded Drug Protection Act
d. Pharmacy Security Act
e. Prescription Drug User Safety Act
A pharmacy that compounds prescription drugs may be eligible for the exemptions
under section 503A of the federal Food, Drug and Cosmetic Act if it complies with
which of the following (select all that apply: there is more than one answer choice
but not all answer choices are correct). - answer>>>a. *Follow CGMP*
b. *Be licensed as a pharmacy under state law*
c. *Compound prescription drugs only for an identified individual patient or in
limited quantities before receipt of a prescription*
d. *Receive a prescription from a licensed practitioner prior to selling a compounded
drug product*
e. charge no more than the wholesale price of the least expensive commercial
available product currently being marketed in the United States
[True/False] Under section 503A of the federal Food, Drug and Cosmetic Act, a
practitioner may obtain a compounded prescription drug from a pharmacy by
issuing a prescription for "office use" in lieu of for an identified individual patient. -
answer>>>*True*
[True/False] Section 503A of the federal Food, Drug and Cosmetic Act prohibits any
person or entity other than a state licensed pharmacy from compounding a
prescription drug product. - answer>>>*True*
,[True/False] If an outsourcing facility compounds prescription drug products for use
in dispensing patientspecific
prescriptions, these products must be compounded in accordance with CGMP
requirements. - answer>>>*True*
Zolpidem is regulated by federal law in the same way as: - answer>>>*Lorazepam*
Labels of commercial drug products that are intended for electrolyte replacement
must contain the concentration ex-pressed in terms of: - answer>>>1.
Milliequivalents
2. Millimoles.
Percogesic is an example of a product that is: - answer>>>Not a controlled substance
Which of the FF are exempt from registration under the Controlled Substance Act? -
answer>>>1. A U. S Army physician
2. A U. S. Public Health Service physician
A customer had a prescription originally fill ...... December1, 2013 ----> January 2,
2014 ------> Earliest date is: - answer>>>12/1/2019 (December 1,2019)
When explaining the Medicare Plan D program to a married couple, the pharmacist
should emphasize: - answer>>>1. The original annual deductible
2. The monthly premium
3. The "donut hole"
The requirement that pharmacists must offer to counsel patients concerning their
prescriptions was included in which of the following congressional actions? -
answer>>>a. Durham-Humphrey Amendment of 1951
b. FD & C Act of 1938
, -
c. *Omnibus Reconciliation Act of 1990*
d. Prescription Drug Marketing Act of 1987
e. Kefauver--Harris Amendment of 1962
A pharmacy chain with stores in several states must obtain: - answer>>>A DEA
number for each individual pharmacy location.
Which of the FF is *not* required to be on the labeling of the prescription container
when the pharmacist fills a Schedule III controlled substance prescription? -
answer>>>*Number of dosage units dispensed*
A physician shares with your pharmacy a topical moisturizing formula which contains
a prescription drug. Which of the following would be appropriate actions for your
pharmacy to take? - answer>>>1. Fill prescriptions written by the physician for 120
grams of this formula.
2. Prepare a pound of the formula in anticipation of additional prescriptions or
refills.
Oral authorization for additional refills on a schedule III prescription are acceptable
as long as: - answer>>>1. The total quantity authorized does not exceed five re-fills
within a six-month period from the date of issue of the original prescription. 2. The
quantity of each additional refill authorized is not greater than the quantity
authorized for the initial filling of the prescription.
Controlled substance prescriptions: - answer>>>1. May be written by typewriter
(except for the prescriber's signature)
2. Must have the name of the physician printed, stamped, typed, or hand-printed on
it.
3. May be prepared by an agent of the prescriber for the prescriber's signature.
VERIFIED CORRECT ANSWERS LATEST 2026-2027
NEW VERSION
A hospital pharmacy is not required to first receive a patient-specific prescription or
order provided that the compounded drug products are only to healthcare facilities
that are owned and controlled the same entity that owns and controls the hospital
pharmacy and that are located within a *............* radius of the compounding
pharmacy - answer>>>*a. 1*
b. 3
c. 10
d. 12
An outsourcing facing that is registered with the FDA and subject to federal oversight
must comply with which of the following requirements (select all that apply: there is
more than one correct answer choice but not all answers choices are correct) -
answer>>>a. *Follow current good manufacturing practices (CGMP)*.
b. *Report adverse events. associated with the compounded drug product.*
c. *Allow FDA access to conduct inspections according to a risk-based schedule*.
d. Receive a prescription from a licensed practitioner prior to selling the
compounded drug
product.
e. Charge no more than the wholesale price of the least expensive commercial
available product currently being marketed in the United States
[True/false] Under section 503A of the federal Food, Drug and Cosmetic Act, a
pharmacy compounding prescription drug products should maintain records of any
calculations performed to determine the limited quantities of drug products
compounded before receipt of a prescription. - answer>>>*True*
, -
The name of the federal law enacted in 2013 in response to an outbreak of
meningitis due to
contamination of pharmacy compounding sterile products is the _____. -
answer>>>a. *Drug Quality and Security Act*
b. Pharmacy Compounding Safety Act
c. Compounded Drug Protection Act
d. Pharmacy Security Act
e. Prescription Drug User Safety Act
A pharmacy that compounds prescription drugs may be eligible for the exemptions
under section 503A of the federal Food, Drug and Cosmetic Act if it complies with
which of the following (select all that apply: there is more than one answer choice
but not all answer choices are correct). - answer>>>a. *Follow CGMP*
b. *Be licensed as a pharmacy under state law*
c. *Compound prescription drugs only for an identified individual patient or in
limited quantities before receipt of a prescription*
d. *Receive a prescription from a licensed practitioner prior to selling a compounded
drug product*
e. charge no more than the wholesale price of the least expensive commercial
available product currently being marketed in the United States
[True/False] Under section 503A of the federal Food, Drug and Cosmetic Act, a
practitioner may obtain a compounded prescription drug from a pharmacy by
issuing a prescription for "office use" in lieu of for an identified individual patient. -
answer>>>*True*
[True/False] Section 503A of the federal Food, Drug and Cosmetic Act prohibits any
person or entity other than a state licensed pharmacy from compounding a
prescription drug product. - answer>>>*True*
,[True/False] If an outsourcing facility compounds prescription drug products for use
in dispensing patientspecific
prescriptions, these products must be compounded in accordance with CGMP
requirements. - answer>>>*True*
Zolpidem is regulated by federal law in the same way as: - answer>>>*Lorazepam*
Labels of commercial drug products that are intended for electrolyte replacement
must contain the concentration ex-pressed in terms of: - answer>>>1.
Milliequivalents
2. Millimoles.
Percogesic is an example of a product that is: - answer>>>Not a controlled substance
Which of the FF are exempt from registration under the Controlled Substance Act? -
answer>>>1. A U. S Army physician
2. A U. S. Public Health Service physician
A customer had a prescription originally fill ...... December1, 2013 ----> January 2,
2014 ------> Earliest date is: - answer>>>12/1/2019 (December 1,2019)
When explaining the Medicare Plan D program to a married couple, the pharmacist
should emphasize: - answer>>>1. The original annual deductible
2. The monthly premium
3. The "donut hole"
The requirement that pharmacists must offer to counsel patients concerning their
prescriptions was included in which of the following congressional actions? -
answer>>>a. Durham-Humphrey Amendment of 1951
b. FD & C Act of 1938
, -
c. *Omnibus Reconciliation Act of 1990*
d. Prescription Drug Marketing Act of 1987
e. Kefauver--Harris Amendment of 1962
A pharmacy chain with stores in several states must obtain: - answer>>>A DEA
number for each individual pharmacy location.
Which of the FF is *not* required to be on the labeling of the prescription container
when the pharmacist fills a Schedule III controlled substance prescription? -
answer>>>*Number of dosage units dispensed*
A physician shares with your pharmacy a topical moisturizing formula which contains
a prescription drug. Which of the following would be appropriate actions for your
pharmacy to take? - answer>>>1. Fill prescriptions written by the physician for 120
grams of this formula.
2. Prepare a pound of the formula in anticipation of additional prescriptions or
refills.
Oral authorization for additional refills on a schedule III prescription are acceptable
as long as: - answer>>>1. The total quantity authorized does not exceed five re-fills
within a six-month period from the date of issue of the original prescription. 2. The
quantity of each additional refill authorized is not greater than the quantity
authorized for the initial filling of the prescription.
Controlled substance prescriptions: - answer>>>1. May be written by typewriter
(except for the prescriber's signature)
2. Must have the name of the physician printed, stamped, typed, or hand-printed on
it.
3. May be prepared by an agent of the prescriber for the prescriber's signature.
