Pharmacy Law Exam MPJE Questions and
Correct Answers (Verified Answers) Plus
Rationales 2026 Q&A | Instant Download Pdf
1. Which federal law requires that a prescription be issued for a
legitimate medical purpose by a practitioner acting in the usual
course of their professional practice?
A) Federal Food, Drug, and Cosmetic Act
B) Controlled Substances Act
C) Poison Prevention Packaging Act
D) Drug Enforcement Administration regulations
Rationale: The Controlled Substances Act (CSA) sets requirements for
prescribing controlled substances for legitimate medical purposes.
Prescribers must act within the usual course of professional practice.
2. Which agency is responsible for enforcing the federal Controlled
Substances Act?
A) FDA
B) DEA
C) CDC
D) USP
,Rationale: The Drug Enforcement Administration (DEA) enforces the
CSA, regulates controlled substances, and issues DEA registration
numbers to practitioners and pharmacies.
3. Which schedule under the CSA includes drugs with no currently
accepted medical use and a high potential for abuse?
A) Schedule II
B) Schedule III
C) Schedule IV
D) Schedule I
Rationale: Schedule I drugs, such as heroin and LSD, have no accepted
medical use in the U.S. and have a high potential for abuse.
4. How often must a pharmacy inventory its Schedule II controlled
substances under federal law?
A) Every year
B) Every month
C) Every 2 years
D) Every 5 years
Rationale: The CSA requires pharmacies to perform a biennial
inventory (every two years) of all controlled substances.
5. Which law governs the safety, efficacy, and labeling of drugs
before they enter interstate commerce?
, A) CSA
B) Poison Prevention Packaging Act
C) Federal Food, Drug, and Cosmetic Act (FDCA)
D) HIPAA
Rationale: The FDCA gives the FDA authority to ensure drugs are safe,
effective, and properly labeled before marketing.
6. What is the maximum day supply for a C-II prescription under
federal law?
A) 30 days
B) 60 days
C) 90 days
D) There is no federal limit; state laws may impose limits
Rationale: Federal law does not specify a maximum day supply for C-II
drugs; state law may restrict this.
7. What form must a pharmacy use to order Schedule II controlled
substances?
A) DEA Form 224
B) DEA Form 106
C) DEA Form 222
D) DEA Form 41
, Rationale: DEA Form 222 is used for purchasing and transferring
Schedule II drugs.
8. Which of the following is NOT required on a prescription label for
a controlled substance?
A) Pharmacy name and address
B) Patient’s insurance provider
C) Prescriber’s name
D) Directions for use
Rationale: Federal law requires patient information, prescriber
information, drug name, and directions, but insurance information is
not mandatory.
9. Which of the following acts regulates the packaging of
prescription drugs for child safety?
A) CSA
B) FDCA
C) HIPAA
D) Poison Prevention Packaging Act
Rationale: The Poison Prevention Packaging Act requires child-
resistant packaging for most prescription and many over-the-counter
medications.
Correct Answers (Verified Answers) Plus
Rationales 2026 Q&A | Instant Download Pdf
1. Which federal law requires that a prescription be issued for a
legitimate medical purpose by a practitioner acting in the usual
course of their professional practice?
A) Federal Food, Drug, and Cosmetic Act
B) Controlled Substances Act
C) Poison Prevention Packaging Act
D) Drug Enforcement Administration regulations
Rationale: The Controlled Substances Act (CSA) sets requirements for
prescribing controlled substances for legitimate medical purposes.
Prescribers must act within the usual course of professional practice.
2. Which agency is responsible for enforcing the federal Controlled
Substances Act?
A) FDA
B) DEA
C) CDC
D) USP
,Rationale: The Drug Enforcement Administration (DEA) enforces the
CSA, regulates controlled substances, and issues DEA registration
numbers to practitioners and pharmacies.
3. Which schedule under the CSA includes drugs with no currently
accepted medical use and a high potential for abuse?
A) Schedule II
B) Schedule III
C) Schedule IV
D) Schedule I
Rationale: Schedule I drugs, such as heroin and LSD, have no accepted
medical use in the U.S. and have a high potential for abuse.
4. How often must a pharmacy inventory its Schedule II controlled
substances under federal law?
A) Every year
B) Every month
C) Every 2 years
D) Every 5 years
Rationale: The CSA requires pharmacies to perform a biennial
inventory (every two years) of all controlled substances.
5. Which law governs the safety, efficacy, and labeling of drugs
before they enter interstate commerce?
, A) CSA
B) Poison Prevention Packaging Act
C) Federal Food, Drug, and Cosmetic Act (FDCA)
D) HIPAA
Rationale: The FDCA gives the FDA authority to ensure drugs are safe,
effective, and properly labeled before marketing.
6. What is the maximum day supply for a C-II prescription under
federal law?
A) 30 days
B) 60 days
C) 90 days
D) There is no federal limit; state laws may impose limits
Rationale: Federal law does not specify a maximum day supply for C-II
drugs; state law may restrict this.
7. What form must a pharmacy use to order Schedule II controlled
substances?
A) DEA Form 224
B) DEA Form 106
C) DEA Form 222
D) DEA Form 41
, Rationale: DEA Form 222 is used for purchasing and transferring
Schedule II drugs.
8. Which of the following is NOT required on a prescription label for
a controlled substance?
A) Pharmacy name and address
B) Patient’s insurance provider
C) Prescriber’s name
D) Directions for use
Rationale: Federal law requires patient information, prescriber
information, drug name, and directions, but insurance information is
not mandatory.
9. Which of the following acts regulates the packaging of
prescription drugs for child safety?
A) CSA
B) FDCA
C) HIPAA
D) Poison Prevention Packaging Act
Rationale: The Poison Prevention Packaging Act requires child-
resistant packaging for most prescription and many over-the-counter
medications.
