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PTU PART 1 ACTUAL EXAM QUESTIONS WITH ANSWERS 2025/2026 GRADED A+

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PTU PART 1 ACTUAL EXAM QUESTIONS WITH ANSWERS 2025/2026 GRADED A+ Mylan's clonazepam 1 mg is AB-rated to Klonopin 1 mg. This means: Select one: Clonazepam can't be substituted for Klonopin Clonazepam is a therapeutic equivalent to Klonopin Clonazepam is a therapeutic alternative to Klonopin Clonazepam is a pharmacologic alternative to Klonopin - Clonazepam is a therapeutic equivalent to Klonopin Which law created two classes of medications, prescription and nonprescription? Select one: Pure Food and Drug Act of 1906 Food, Drug, and Cosmetic Act of 1938 Durham-Humphrey Amendment of 1951 Omnibus Budget Reconciliation Act of 1990 - Durham-Humphrey Amendment of 1951 NDC numbers consist of: Select one: 10 digits divided into 3 segments 13 digits divided into 3 segments 10 digits divided into 5 segments 13 digits divided into 5 segments - 10 digits divided into 3 segments Which is an example of a medication that is part of a Class II recall?

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PTU PART 1 QUESTIONS WITH ANSWERS 2025/2026
GRADED A+
Your pharmacy stocks 100-count bottles of diazepam. According to federal law, during
inventory, the pharmacy must have a(n):
Select one:
Exact count of diazepam
Virtual count of diazepam
Perpetual count of diazepam
Estimated count of diazepam - Estimated count of diazepam

What is an investigational drug?
Select one:
A drug compound undergoing theoretical tests
A drug compound undergoing tests to determine its use
A drug compound undergoing clinical testing in humans
A drug compound undergoing clinical testing in animals - A drug compound undergoing
clinical testing in humans

Which controlled substance medication has the most stringent requirements in the
pharmacy?
Select one:
Kadian
Klonopin
Provigil
Robitussin AC - Kadian

Patient package inserts contain information about the:
Select one:
Role of Food and Drug Administration
Benefits and risks of using a medication
Dispensing requirements for controlled substances
Packaging requirements to protect children from harmful meds - Benefits and risks of
using a medication

FDA-approved handouts that inform patients about risks of drugs that pose the most
significant and serious health concerns are called:
Select one:
Medication guides
Patient package inserts
Consumer medication leaflets
Protected health information sheets - Medication guides

For meds that require a Medication Guide, you must give one:
Select one:
With all outpatient prescriptions

,Only when an outpatient is receiving a new prescription
When the patient signs a medication guide authorization form
Only when the prescriber writes "MedGuide required" on the face of the prescription -
With all outpatient prescriptions

Federal law says that you can only refill an Rx for a Schedule III controlled substance 5
times in 6 months. Your state law says that you can only refill an Rx for a Schedule III
controlled substance 4 times in 6 months. What is the maximum number of refills you
can dispense for a Schedule III controlled substance Rx?
Select one:
4
5
6
12 - 4

According to federal law, in most cases, an oxycodone prescription can be:
Select one:
Verbal or faxed
Electronic or written
Electronic, written, or faxed
Verbal, electronic, written, or faxed - Electronic or written

Which type of recall involves products that are unlikely to cause adverse effects?
Select one:
Class I recall
Class II recall
Class III recall
Market withdrawal - Class III recall

The NDC for Nexium 40 mg is 0186-5040-31. The number "0186" identifies:
Select one:
Dosage form
Manufacturer
Medication name
Package size - Manufacturer

Which schedule of controlled substances is Ambien classified under?
Select one:
II
III
IV
V - IV

Which is a principle of HIPAA?
Select one:
To counsel patients on new and refill prescription medications

,To dispense prescription medications with child-resistant packaging
To dispense certain prescription medications with a Medication Guide
To use and disclose the minimum necessary amount of protected information - Which is
a principle of HIPAA?
Select one:
To counsel patients on new and refill prescription medications
To dispense prescription medications with child-resistant packaging
To dispense certain prescription medications with a Medication Guide
To use and disclose the minimum necessary amount of protected information

The Omnibus Reconciliation Act of 1990 requires:
Select one:
Each new medication to have a national drug code
The pharmacist to consult about prescriptions with patients
Dietary supplements to be treated more like drugs than food
Oral contraceptives to be dispensed with a patient package insert - The pharmacist to
consult about prescriptions with patients

Which resource contains TE codes to help guide generic substitution?
Select one:
Blue Book
Orange Book
Red Book
Yellow Book - Orange Book

Investigational drug returns may be performed by the:
Select one:
Drug manufacturer
Drug sponsor
IDS technician
Nursing staff - IDS technician

Which medication is a Schedule V controlled substance?
Select one:
Lomotil
Lopressor
Lortab
Lunesta - Lomotil

According to the Poison Prevention Packaging Act of 1970, a Symbicort inhaler:
Select one:
Is considered an adulterated product
Must be dispensed with a patient package insert
Can be dispensed in a child-resistant container
Can be dispensed in a non-child-resistant container - Can be dispensed in a non-child-
resistant container

, Who usually makes the decision to recall a drug product?
Select one:
DEA
Drug company
FDA
Pharmacist - Drug company

According to the Poison Prevention Act of 1970, which medication class can be
dispensed in a non-child-resistant package in an outpatient setting?
Select one:
Antidepressants
Antihypertensives
Opioids
Oral contraceptives - Oral contraceptives

A generic product has the same active ingredient, strength, and dosage form as the
brand-name product. If this generic also absorbs and releases the same as the brand-
name drug, it is considered a:
Select one:
Pharmacologic alternative
Pharmacologic equivalent
Therapeutic alternative
Therapeutic equivalent - Therapeutic equivalent

Which is an example of a Class I recall?
Select one:
An oral medication that smells moldy
An injectable med labeled with the wrong package size
An injectable med with pieces of glass in the medication
An oral medication that didnt go through the modern FDA-approval process - An
injectable med with pieces of glass in the medication

According to HIPAA, a patient's lab results are considered:
Select one:
BOP
PPI
PHI
REMS - PHI

Which medication must be accompanied by a patient package insert?
Select one:
Cenestin
Cialis
Coumadin
Crestor - Cenestin

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