PTU RITE AID EXAM 2024-2025 WITH
ACTUAL CORRECT QUESTIONS AND
VERIFIED DETAILED ANSWERS
|FREQUENTLY TESTED QUESTIONS AND
SOLUTIONS |ALREADY GRADED
A+|NEWEST|GUARANTEED PASS |LATEST
UPDATE
The Health Insurance Portability and Accountability Act of 1996
Governs patient privacy and the sharing of patient information
Each new drug is required to have an NDC number according to the
Drug Listing Act of 1972
DSHEA requires that a
Dietary supplement must make true claims
Which federal agency is responsible for the regulation of labeling on prescription and over-the-counter
medications
FDA
Which law requires pharmaceutical manufacturers to prove a drug's purity, strength, and before it can
be sold
Food, Drug, and Cosmetic Act of 1938
For a medication's packaging to be considered child-resistant, it
Cannot be opened by 80% of children younger than 5 years of age, but can be opened by 90% of adults
According to HIPAA, when you use and disclose only the amount of protected patient information
needed, it is known as
minimum necessary rule
Which law requires the pharmacist to consult about new prescriptions with patients
1|Page
,OBRA 90
According to the Poison Prevention Act of 1970, which medication class can be dispensed in a non-child-
resistant package in an outpatient setting
oral contraceptives
FDA-approved handouts that inform patients about risks of drugs that pose the most significant and
serious health concerns are called
Medication guides
Which section of the NDC identifies the name, strength, and dosage form of the medication
second
A 10-digit number divided into three segments located on a medication container is known as the
National Drug Code
The Poison Prevention Packaging Act of 1970 is responsible for requiring
Child-resistant caps on prescriptions
Which governmental agency publishes the immunization requirements for children and adults each year
CDC
According to HIPAA, which is considered protect health information
Patients prescription records
Which medication must be dispensed with a patient package insert
estrogen
Which law created two classes of medications, prescription and nonprescription
Durham-Humphrey Amendment of 1951
Which section of the NDC number identifies package size and type
third
Federal law says that your pharmacy must complete a controlled substance inventory once eery two
years. Your state law says that your pharmacy must complete a controlled substance inventory every
year. Ow often should your pharmacy complete a controlled substance inventory?
Once a year
When Mr. Reynold's picks up his prescriptions, he tears off the tag and medication information sheet for
you to disposed of. Since the paperwork has Mr. Reynold's name, phone number, and medication name
on it, how would you dispose of it
Put it in the trash bin labeled for shredding
2|Page
,The Hatch-Waxman Act is also known as the:
Drug Price Competition and Patent Term
Restoration Act of 1984
According to the Poison Prevention Packaging Act of 1970, which medication can be dispensed in a non-
child-resistant package in an outpatient setting?
Sublingual nitroglycerin tablets
To bring a generic medication to market, a manufacturer must submit a
Abbreviated New Drug Application
Which organization must the Investigational New Drug application be filed with
FDA
Which type of drug is involved in a Class III (3) recall
Drugs unlikely to cause adverse events
Which DAW code means that substitution is not allowed by the prescribe
1
A brand-name drug that is relabeled and marketed under a generic product name is a
Authorized generic
Which committee approves patient consent forms and protects the welfare of drug search volunteers
IRB
What are the 3 phases an investigational drug goes through prior to submitting a New Drug Application
Phase 1,2,3
Which resource contains TE codes to help guide generic substitution
Orange Book
DAW 3 means
Substitution is not allowed by the pharmacist
A therapeutic alternative is a drug that
Contains a different active ingredient, but is in the same drug class and works similarly
Which is an example of a medication that is par of a Class II (2) recall
A contaminated medication that could cause temporary, but reversible adverse effects
Which involves introducing a drug for the first time in humans
3|Page
, Phase 1 Testing
A pharmacologic alternative is a drug that
Contains the same active ingredient, but is a different strength
A collaborative agreement is a system that allows pharmacist to automatically substitute
Pharmacologic and therapeutic alternatives
Which DAW code means that substitution is not allowed since the dispensing of the brand-name drug is
mandated by law
DAW 7
A drug is usually permanently withdrawn from the market because it is considered
harmful
Topmax is an immediate-release topiramate tablet. Trokendi XR is an extended-release topiramate
tablet. Both medications are used to treat the same condition. Topamax and tTrokendi XR are
Pharmacological alternatives
Which is an example of a Class I (1) recall
An injectable med with pieces of glass in the medication
Mylan's clonazepam 1 mg is AB-rated to Klonopin 1mg. This means
Clonazepam is a therapeutic equivalent to Klonopin
What does DAW 5 mean
Brand-name is dispensed as generic
A brand-name patent gives a
Drug company exclusive rights to the compound for a limited time
Which responsibility may be performed by an IDS technician
Drug preparation
DAW 2 means
Substitution is allowed by the prescriber, but the patient requested the brand-name product to be
dispensed
When a generic medication is identical in active ingredient, strength, dosage form, and routed of
administration as the brand-name product, it is considered a(n)
Pharmaceutical equivalent
DAW 6 means
4|Page
ACTUAL CORRECT QUESTIONS AND
VERIFIED DETAILED ANSWERS
|FREQUENTLY TESTED QUESTIONS AND
SOLUTIONS |ALREADY GRADED
A+|NEWEST|GUARANTEED PASS |LATEST
UPDATE
The Health Insurance Portability and Accountability Act of 1996
Governs patient privacy and the sharing of patient information
Each new drug is required to have an NDC number according to the
Drug Listing Act of 1972
DSHEA requires that a
Dietary supplement must make true claims
Which federal agency is responsible for the regulation of labeling on prescription and over-the-counter
medications
FDA
Which law requires pharmaceutical manufacturers to prove a drug's purity, strength, and before it can
be sold
Food, Drug, and Cosmetic Act of 1938
For a medication's packaging to be considered child-resistant, it
Cannot be opened by 80% of children younger than 5 years of age, but can be opened by 90% of adults
According to HIPAA, when you use and disclose only the amount of protected patient information
needed, it is known as
minimum necessary rule
Which law requires the pharmacist to consult about new prescriptions with patients
1|Page
,OBRA 90
According to the Poison Prevention Act of 1970, which medication class can be dispensed in a non-child-
resistant package in an outpatient setting
oral contraceptives
FDA-approved handouts that inform patients about risks of drugs that pose the most significant and
serious health concerns are called
Medication guides
Which section of the NDC identifies the name, strength, and dosage form of the medication
second
A 10-digit number divided into three segments located on a medication container is known as the
National Drug Code
The Poison Prevention Packaging Act of 1970 is responsible for requiring
Child-resistant caps on prescriptions
Which governmental agency publishes the immunization requirements for children and adults each year
CDC
According to HIPAA, which is considered protect health information
Patients prescription records
Which medication must be dispensed with a patient package insert
estrogen
Which law created two classes of medications, prescription and nonprescription
Durham-Humphrey Amendment of 1951
Which section of the NDC number identifies package size and type
third
Federal law says that your pharmacy must complete a controlled substance inventory once eery two
years. Your state law says that your pharmacy must complete a controlled substance inventory every
year. Ow often should your pharmacy complete a controlled substance inventory?
Once a year
When Mr. Reynold's picks up his prescriptions, he tears off the tag and medication information sheet for
you to disposed of. Since the paperwork has Mr. Reynold's name, phone number, and medication name
on it, how would you dispose of it
Put it in the trash bin labeled for shredding
2|Page
,The Hatch-Waxman Act is also known as the:
Drug Price Competition and Patent Term
Restoration Act of 1984
According to the Poison Prevention Packaging Act of 1970, which medication can be dispensed in a non-
child-resistant package in an outpatient setting?
Sublingual nitroglycerin tablets
To bring a generic medication to market, a manufacturer must submit a
Abbreviated New Drug Application
Which organization must the Investigational New Drug application be filed with
FDA
Which type of drug is involved in a Class III (3) recall
Drugs unlikely to cause adverse events
Which DAW code means that substitution is not allowed by the prescribe
1
A brand-name drug that is relabeled and marketed under a generic product name is a
Authorized generic
Which committee approves patient consent forms and protects the welfare of drug search volunteers
IRB
What are the 3 phases an investigational drug goes through prior to submitting a New Drug Application
Phase 1,2,3
Which resource contains TE codes to help guide generic substitution
Orange Book
DAW 3 means
Substitution is not allowed by the pharmacist
A therapeutic alternative is a drug that
Contains a different active ingredient, but is in the same drug class and works similarly
Which is an example of a medication that is par of a Class II (2) recall
A contaminated medication that could cause temporary, but reversible adverse effects
Which involves introducing a drug for the first time in humans
3|Page
, Phase 1 Testing
A pharmacologic alternative is a drug that
Contains the same active ingredient, but is a different strength
A collaborative agreement is a system that allows pharmacist to automatically substitute
Pharmacologic and therapeutic alternatives
Which DAW code means that substitution is not allowed since the dispensing of the brand-name drug is
mandated by law
DAW 7
A drug is usually permanently withdrawn from the market because it is considered
harmful
Topmax is an immediate-release topiramate tablet. Trokendi XR is an extended-release topiramate
tablet. Both medications are used to treat the same condition. Topamax and tTrokendi XR are
Pharmacological alternatives
Which is an example of a Class I (1) recall
An injectable med with pieces of glass in the medication
Mylan's clonazepam 1 mg is AB-rated to Klonopin 1mg. This means
Clonazepam is a therapeutic equivalent to Klonopin
What does DAW 5 mean
Brand-name is dispensed as generic
A brand-name patent gives a
Drug company exclusive rights to the compound for a limited time
Which responsibility may be performed by an IDS technician
Drug preparation
DAW 2 means
Substitution is allowed by the prescriber, but the patient requested the brand-name product to be
dispensed
When a generic medication is identical in active ingredient, strength, dosage form, and routed of
administration as the brand-name product, it is considered a(n)
Pharmaceutical equivalent
DAW 6 means
4|Page
