299+ Free DE MPJE Practice Questions

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Under the Controlled Substances Act (CSA), which DEA schedule includes drugs with the highest potential for abuse and no currently accepted medical use?

Schedule I

Schedule II

Schedule III

Schedule IV

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Free MPJE Practice Test by State 2026: 5,000+ Pharmacy Law Questions18 min read

2026 Statistics

Key Facts: DE MPJE Exam

120

Questions

100 scored + 20 pretest

Passing Score

NABP scaled score

2.5h

Exam Time

Pearson VUE

4:1

Tech Ratio

DE max

30h/2yr

CE Required

DE renewal

$270

Exam Fee

NABP 2026

The DE MPJE covers federal pharmacy law (DEA, FDA, CSA, HIPAA) and Delaware-specific regulations including PDMP mandatory checks, 7-day initial opioid limit, naloxone standing orders, collaborative practice agreements, telepharmacy regulations, 30h/2yr CE, and 4:1 technician ratio.

Sample DE MPJE Practice Questions

Try these sample questions to test your DE MPJE exam readiness. Each question includes a detailed explanation. Start the interactive quiz above for the full 299+ question experience with AI tutoring.

1Under the Controlled Substances Act (CSA), which DEA schedule includes drugs with the highest potential for abuse and no currently accepted medical use?

A.Schedule I

B.Schedule II

C.Schedule III

D.Schedule IV

Explanation: Schedule I substances have a high potential for abuse, no currently accepted medical use in treatment in the United States, and a lack of accepted safety for use under medical supervision. Examples include heroin, LSD, and MDMA.

2A DEA Form 222 is required for the transfer of which schedule of controlled substances between registrants?

A.Schedule II only

B.Schedules II and III

C.Schedules III through V

D.All controlled substances

Explanation: DEA Form 222 (or its electronic equivalent under CSOS) is required for the distribution and transfer of Schedule II controlled substances between DEA registrants. Schedules III-V can be transferred using invoices with specific record-keeping requirements.

3Under federal law, what is the maximum number of refills allowed for a Schedule III controlled substance prescription?

A.No refills allowed

B.Up to 3 refills within 6 months

C.Up to 5 refills within 6 months

D.Up to 5 refills within 1 year

Explanation: Federal law allows up to 5 refills for Schedule III-V controlled substance prescriptions within 6 months from the date the prescription was issued. Schedule II prescriptions cannot be refilled.

4The Durham-Humphrey Amendment of 1951 established which key distinction in drug classification?

A.Generic vs. brand-name drugs

B.Prescription (legend) vs. over-the-counter drugs

C.Controlled vs. non-controlled substances

D.Biological vs. chemical drugs

Explanation: The Durham-Humphrey Amendment to the Federal Food, Drug, and Cosmetic Act (FDCA) established the distinction between prescription (legend) drugs and over-the-counter (OTC) drugs.

5Under OBRA '90, pharmacists participating in Medicaid programs are required to perform which of the following?

A.Drug utilization review and patient counseling

B.Compounding of specialty medications

C.Verification of patient insurance

D.Annual inventory of controlled substances

Explanation: The Omnibus Budget Reconciliation Act of 1990 (OBRA '90) mandated that pharmacists provide drug utilization review (DUR) and offer to counsel Medicaid patients on their prescriptions.

6The Poison Prevention Packaging Act (PPPA) requires child-resistant packaging for most prescription drugs. Which of the following is an exemption?

A.Sublingual nitroglycerin tablets

B.Amoxicillin capsules

C.Metformin tablets

D.Lisinopril tablets

Explanation: Sublingual nitroglycerin tablets are exempt from child-resistant packaging requirements under the PPPA because they require immediate access in emergency cardiac situations.

7What is the primary purpose of the Drug Supply Chain Security Act (DSCSA)?

A.Regulate direct-to-consumer advertising

B.Create an electronic system to track and trace prescription drugs

C.Establish drug pricing transparency

D.Monitor pharmacy benefit manager practices

Explanation: The DSCSA establishes requirements for an electronic, interoperable system to identify and trace certain prescription drugs as they are distributed in the United States to protect consumers from exposure to drugs that may be counterfeit, stolen, contaminated, or otherwise harmful.

8Under HIPAA, a pharmacy may disclose protected health information (PHI) without patient authorization for which purpose?

A.Marketing of new pharmaceutical products

B.Treatment, payment, and healthcare operations

C.Employment background checks

D.Sale of patient mailing lists

Explanation: HIPAA permits disclosure of PHI without patient authorization for treatment, payment, and healthcare operations (TPO). Other disclosures generally require written patient authorization.

9How often must a pharmacy conduct an inventory of Schedule II controlled substances according to DEA regulations?

A.Monthly

B.Quarterly

C.Biennially (every 2 years)

D.Annually

Explanation: DEA regulations require a complete inventory of all controlled substances (Schedules II-V) at least every two years (biennially). The initial inventory must be taken on the date the registrant first engages in the activity.

10A pharmacist discovers a significant loss of Schedule II controlled substances. Which DEA form must be filed?

A.DEA Form 41

B.DEA Form 106

C.DEA Form 222

D.DEA Form 224

Explanation: DEA Form 106 (Report of Theft or Significant Loss of Controlled Substances) must be filed when a pharmacy discovers a significant loss or theft of controlled substances.

About the DE MPJE Exam

The Delaware MPJE tests knowledge of federal pharmacy law and Delaware-specific pharmacy regulations under Del. Code Title 24 Chapter 25. Required alongside the NAPLEX for pharmacist licensure in Delaware.

Questions

120 scored questions

Time Limit

2.5 hours

Passing Score

75 (scaled score)

Exam Fee

$270 (NABP / DE Board of Pharmacy)

DE MPJE Exam Content Outline

22%

Licensure & Personnel

Pharmacist qualifications, intern/technician requirements, license renewal, disciplinary actions

33%

Pharmacist Practice

Prescription requirements, counseling, controlled substance rules, collaborative practice agreements

24%

Dispensing Requirements

Generic substitution, prescription transfers, DUR, labeling, PDMP checking

21%

Pharmacy Operations

Controlled substance records, compounding standards, pharmacy permits, automated dispensing

How to Pass the DE MPJE Exam

What You Need to Know

Passing score: 75 (scaled score)
Exam length: 120 questions
Time limit: 2.5 hours
Exam fee: $270

Keys to Passing

Complete 500+ practice questions
Score 80%+ consistently before scheduling
Focus on highest-weighted sections
Use our AI tutor for tough concepts

DE MPJE Study Tips from Top Performers

1Study Del. Code Title 24 Chapter 25 for Delaware-specific pharmacy regulations

2Master DEA controlled substance schedules, forms (222, 106, 41), and corresponding responsibility

3Know Delaware PDMP requirements and mandatory query triggers

4Review Delaware naloxone standing order and collaborative practice agreements

5Understand federal vs. state law conflicts — the more restrictive law prevails

Frequently Asked Questions

What is the DE MPJE passing score?

The Delaware MPJE requires a scaled score of 75. The exam has 120 questions (100 scored, 20 pretest) over 2.5 hours at Pearson VUE.

What Delaware laws are tested?

The DE MPJE covers Del. Code Title 24 Chapter 25, Board of Pharmacy rules, PDMP requirements, and state-specific dispensing/controlled substance regulations.

What is the technician ratio in Delaware?

Delaware allows a 4:1 technician-to-pharmacist ratio. Technicians must be registered with the Delaware Board of Pharmacy.

How many CE hours does Delaware require?

Delaware requires 30 hours per 2-year renewal period of ACPE-accredited continuing pharmacy education.

What is Delaware's opioid supply limit?

Delaware limits initial opioid prescriptions for acute pain to a 7-day supply.