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FPGEE MANAGEMENT EXAM 2024/2025 QUESTIONS & ANSWERS $16.49   Add to cart

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FPGEE MANAGEMENT EXAM 2024/2025 QUESTIONS & ANSWERS

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FPGEE MANAGEMENT EXAM 2024/2025 QUESTIONS & ANSWERS

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  • September 18, 2024
  • 69
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • FPGEE MANAGEMENT
  • FPGEE MANAGEMENT
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YANCHY
FPGEE MANAGEMENT EXAM 2024/2025
QUESTIONS & ANSWERS


Pseudoephedrine is (a)n ................ - Precise Answer ✔✔a. Analogue
b. *Precursor*


[True/false]: Cocaine is a narcotic substance? - Precise Answer
✔✔*True*


A pharmacy may not sell more than *................* grams of
methamphetamine precursor in *........* days - Precise Answer ✔✔a.
3.37/7
b. 4.85/10
c. *5.76/30*


Postmarketing surveillance of a drug product is referred to as
*..................* - Precise Answer ✔✔a. Phase 1
b. Phase 2
c. Phase 3
d. *Phase 4*


The (United States Adopted Names) [*USAN*] designates which of the
following (select all that apply): - Precise Answer ✔✔a. Brand name
b. *Generic name*

,c. *Nonproprietary*
d. Proprietory


Which of the following is *not* a sponsor of USAN? - Precise Answer
✔✔a. AMA
b. APhA
c. *FDA*
d. USP


[True/False]: USAN is the final authority/approval for new drug names:
- Precise Answer ✔✔*False*


The drug price competition and Patent Term Restoration Act provides
up to an additional ............... of the patent product. - Precise Answer
✔✔a. 6 months
b. 1 year
c. 3 years
d. *5 years*
e. 7 years


A drug product has the following NDC: *1074012804* For newer drugs,
the: - Precise Answer ✔✔a. 10740 - Manufacturer
b. 12804 - Drug in package

,[True/False]: CGMP applies only to sterile product manufacturing. -
Precise Answer ✔✔*False*


The FDA unit that oversee prescription drug advertising is *............* -
Precise Answer ✔✔a. DDMAC
b. *OPDP*
[*OPDP* = Office of Prescription Drug Promotion]


[True/False]: The imprint requirement for solid oral dosage units applies
only to tablets. - Precise Answer ✔✔*False*


Which of the following is not a part of *PDMA* [Prescription Drug
Marketing Act of 1987] - Precise Answer ✔✔a. Distribution channels.
b. Reimportation
c. Samples and coupons
d. Resale of pharmaceuticals.
e. *None of the above*


[True/False]: Manufacturers of prescription drugs may distribute
information about off-label uses of their drugs - Precise Answer
✔✔*True*


[True/False]: Unit dose drug commercial packaging is subject to the
same requirements as bulk drug commercial packaging. - Precise
Answer ✔✔*False*

, Unit dose drug packaging performed by a practitioner should not exceed
25% of the remaining time between the date of repackaging and the
original expiration date or *...............* months from the date of
repackaging, whichever is *................*. - Precise Answer ✔✔*12
month ; Less (the least)*


In order for a consumer to be eligible for appointment to the board, they
must be a resident of TN for ........ years. - Precise Answer ✔✔*5*


Violating the Tennessee pharmacy practice Act shall be classified as a
class ....... misdemeanor: - Precise Answer ✔✔*Class C*


If authorization is not obtained within the first 72 hour supply how many
additional day supplies are you allowed to dispense: - Precise Answer
✔✔* 3 days*


[True/False]: In regards to hormonal contraceptives, pharmacists under a
collaborative practice agreement are only allowed to provide to
individuals that are 18 years of age or older. - Precise Answer
✔✔*False*


A change of licensure address must be reported within .......... of change.
- Precise Answer ✔✔*30 days*


A health care provider will be revoked if the renewal fee is not paid
within .......... of the due date. - Precise Answer ✔✔*60 days*

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