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Quizzes > Health & Medicine > Human Anatomy & Medicine

Take the Indiana Pharmacy Law MPJE Quiz Now

Ready to ace the Indiana MPJE? Try free MPJE sample questions now!

Difficulty: Moderate
2-5mins
Learning OutcomesCheat Sheet
Paper art style quiz Indiana Pharmacy Law MPJE practice questions with prescription icons, books on sky blue background

This quiz helps you practice Indiana pharmacy law for the MPJE and check gaps before the exam. Work through questions on prescriptions, drug definitions, and record‑keeping in an exam‑like format at your pace. Want more practice? Try more pharmacy practice questions.

Which state agency issues and renews pharmacy licenses in Indiana?
Indiana Board of Pharmacy
Indiana Department of Revenue
Department of Motor Vehicles
State Board of Health
In Indiana, the Board of Pharmacy is the regulatory authority responsible for issuing and renewing pharmacy licenses. They set the standards for safe pharmacy practice and monitor compliance with state law. All pharmacists and pharmacies must be licensed through this board to operate legally.
How many years must a pharmacy maintain prescription records in Indiana?
10 years
2 years
5 years
1 year
Indiana law requires that pharmacies retain prescription records, including controlled substances, for at least two years. This retention period helps ensure that patient history is accessible for audits and safety reviews. Records can be stored electronically or in hard copy.
Who may legally compound and dispense medications in an Indiana pharmacy?
Pharmacy technician
Pharmacist
Nursing home director
Store manager
Only a licensed pharmacist is authorized to compound and dispense medications under Indiana law. Pharmacy technicians and other personnel may assist under the direct supervision of a pharmacist, but the pharmacist retains ultimate responsibility. This ensures patient safety and proper pharmaceutical practice.
What is the maximum number of pharmacist-intern trainees a supervising pharmacist may mentor at one time in Indiana?
4
2
3
1
Indiana regulations allow a licensed pharmacist to supervise up to two pharmacy interns simultaneously. This limit ensures that the supervising pharmacist can adequately oversee training and maintain patient safety. Exceeding this number would violate state internship rules.
Which of the following elements is required on every prescription label in Indiana?
Drug expiration date
NDC number of the drug
Pharmacy name and address
Prescriber's Social Security number
Indiana law mandates that every dispensed prescription label include the pharmacy's name and address to ensure traceability and patient safety. Other required elements include patient name, drug name, strength, and directions for use. Additional elements may be required under federal law.
Under Indiana law, must a pharmacist be present on the premises of a pharmacy during all operating hours?
Only during business hours
Only on weekdays
No, presence is optional
Yes, at all times during operating hours
Indiana regulations require that a licensed pharmacist be on-site during all times the pharmacy is open to the public. This ensures continuous professional oversight and patient safety. Operating without a pharmacist present is not permitted.
Which professional is authorized to administer vaccines in an Indiana pharmacy?
Pharmacist
Pharmacy technician
Medical assistant
Dentist
In Indiana, licensed pharmacists are authorized to administer vaccines after completing state-approved training. Pharmacy technicians and other personnel may assist but cannot independently administer. This authority improves vaccination access across the state.
What is the legal age to purchase non-prescription syringes without a prescription in Indiana?
18 years
21 years
No age restriction
16 years
Indiana law allows individuals aged 18 and older to purchase non-prescription syringes at pharmacies without a prescription. This regulation aims to reduce communicable disease transmission. Pharmacies must still follow state reporting and record-keeping requirements.
A pharmacy technician in Indiana must be at least how old to qualify for registration?
18 years
20 years
21 years
16 years
Indiana requires pharmacy technician applicants to be at least 18 years old. This ensures a minimum level of maturity and responsibility for handling sensitive pharmacy tasks. Technicians must also meet education and training standards.
Which of the following is classified as a Schedule II controlled substance in Indiana?
Marijuana
Codeine with acetaminophen (?90 mg)
Diazepam
Oxycodone
Oxycodone is listed as a Schedule II controlled substance due to its high potential for abuse and dependence. Diazepam is Schedule IV, lower risk. Codeine combinations under 90 mg are Schedule III. Marijuana remains Schedule I at the federal level.
What is the standard timeframe to report significant loss or theft of controlled substances in Indiana?
72 hours
One week
48 hours
24 hours
Indiana law requires that any significant theft or loss of controlled substances be reported to the Board of Pharmacy within 24 hours of discovery. This rapid reporting helps prevent diversion and enables swift investigation. A DEA Form 106 must accompany the report.
Under Indiana law, how many hours of continuing education must a pharmacist complete biennially?
20 hours
30 hours
12 hours
40 hours
Pharmacists in Indiana must complete 30 hours of continuing education every two years to maintain licensure. Of those, at least two hours must cover Indiana pharmacy law. The Board audits CE records to ensure compliance.
How much of a controlled substance may a pharmacist dispense on an emergency refill if the prescriber is unavailable?
7-day supply
30-day supply
24-hour supply
72-hour supply
Indiana allows pharmacists to dispense up to a 72-hour supply of a non-controlled prescription in an emergency when the prescriber cannot be reached. For controlled substances, emergency fills are more restrictive. Documentation must be kept in the patient's record.
Which schedule contains anabolic steroids under Indiana law?
Schedule IV
Schedule V
Schedule III
Schedule II
Anabolic steroids are classified as Schedule III controlled substances due to their moderate to low potential for physical and psychological dependence. Indiana aligns with federal scheduling on this issue. Physicians must follow specific prescribing requirements.
How many times may a prescription for a non-controlled substance be transferred between pharmacies in Indiana?
Twice
Once
Up to 5 times
Unlimited
Non-controlled substance prescriptions may be transferred an unlimited number of times between pharmacies, provided both parties maintain proper records of the transfer. Controlled substance transfers are limited by schedule. All transfers must comply with state transfer record requirements.
What is the validity period for a controlled substance prescription in Indiana?
90 days
30 days
One year
Six months
Controlled substance prescriptions in Indiana are valid for up to one year from the date they are written, except for Schedule II opioids for acute pain which may have additional restrictions. Pharmacists should verify state and federal guidelines for specific schedules.
Which form must a pharmacy complete when disposing of controlled substances in Indiana?
DEA Form 222
DEA Form 106
DEA Form 41
DEA Form 224
DEA Form 41 is used to report the destruction of controlled substances. It documents quantities, methods of disposal, and witness signatures. Pharmacies must retain this form for at least two years.
Which federal act requires pharmacies to offer patient counseling on new prescriptions?
Durham-Humphrey Amendment
FDCA
HIPAA
OBRA '90
The Omnibus Budget Reconciliation Act of 1990 (OBRA '90) mandates that pharmacists offer counseling to Medicaid patients on new prescriptions. Many states, including Indiana, have extended this requirement to all patients. Counseling improves medication adherence and safety.
How often must a pharmacist inspect automated dispensing machines in Indiana?
Quarterly
Monthly
Annually
Weekly
Indiana regulations require pharmacists to conduct quarterly inspections of automated dispensing machines to ensure proper operation, security, and record accuracy. Documentation of each inspection must be maintained for audit purposes.
When substituting a generic drug for a brand-name prescription in Indiana, the label must include which phrase?
Equivalent to [brand-name]
Generic substitute
Generic for [brand-name]
May differ from brand
Indiana law requires that prescription labels clearly state "Generic for [brand-name]" when a pharmacist substitutes a generic equivalent. This transparency ensures patient awareness of the dispensed product.
Who may sign a DEA Form 222 for ordering Schedule II substances in Indiana?
Pharmacy intern
Any licensed pharmacist
An authorized DEA registrant
Pharmacy technician
Only the individual whose signature appears on the DEA registration or someone granted power of attorney by that registrant may sign DEA Form 222. This process ensures accountability and compliance with controlled substance ordering.
Within how many days must a change of pharmacist-in-charge (PIC) be reported to the Indiana Board of Pharmacy?
Immediately
10 days
30 days
60 days
Indiana law requires that a change in pharmacist-in-charge be reported to the Board within 30 days of the effective date. This notification allows the Board to update records and ensures continuous oversight of pharmacy operations.
A prescription for a controlled substance written by a veterinarian in Indiana must include which additional information?
Owner's Social Security number
Clinic's DEA registration
Owner's date of birth
Species of the animal
Veterinary prescriptions for controlled substances must indicate the species of animal to ensure proper dosing and record keeping. This requirement distinguishes veterinary use from human dispensing.
A prescriber may issue multiple Schedule II prescriptions at once for a patient's 90-day supply provided each is dated on a different day. What is the maximum cumulative supply allowed?
60 days
90 days
30 days
120 days
Federal and Indiana law allow a prescriber to issue multiple Schedule II prescriptions for up to a 90-day supply, as long as each prescription is dated and written on a separate day. This provision helps reduce patient visits while maintaining controlled substance safeguards.
Under Indiana law, how often must a pharmacy perform a complete inventory of controlled substances?
Every year
Every five years
Every six months
Every two years
Indiana statutes require a biennial (every two years) complete inventory of all controlled substances on hand. Partial inventories are required when new schedules are added. Proper documentation ensures compliance and helps detect diversion.
How soon must a retail pharmacy receive a central fill prescription order after sending the original for non-controlled substances?
72 hours
24 hours
48 hours
8 hours
When a retail pharmacy sends a non-controlled prescription to a central fill pharmacy, the filled prescription must be returned within 24 hours. This timeframe ensures timely patient access to medications. The prescription label must indicate the central fill origin.
What is the maximum amount of pseudoephedrine base a person can purchase in one day in Indiana?
7.5 grams
3.6 grams
9 grams
2 grams
Indiana law limits a purchaser to 3.6 grams of pseudoephedrine base per 24-hour period. This restriction helps prevent the illicit manufacture of methamphetamine. Sellers must verify ID and log transactions.
Who is responsible for supervising a sterile compounding facility in Indiana?
Physician
Pharmacy technician
Licensed pharmacist
Registered nurse
A licensed pharmacist with sterile compounding training must supervise all sterile compounding activities in Indiana. They ensure compliance with USP <797> standards and state regulations. Proper oversight is critical for patient safety.
How long must a pharmacy retain procurement records of controlled substances in Indiana?
Ten years
One year
Two years
Five years
Procurement records for controlled substances, including invoices and DEA Form 222 copies, must be kept for at least two years in Indiana. This aligns with federal DEA requirements and helps facilitate inspections.
Which federal statute prohibits dispensing drugs that are misbranded or adulterated?
Harrison Narcotics Tax Act
Federal Food, Drug, and Cosmetic Act
Tamper-Resistant Packaging Act
Durham-Humphrey Amendment
The Federal Food, Drug, and Cosmetic Act (FDCA) outlaws the sale of adulterated or misbranded drugs in interstate commerce. It establishes definitions and standards for drug safety and labeling. Violations can lead to enforcement actions.
What is the maximum term length for a collaborative practice agreement in Indiana?
Two years
Five years
Three years
One year
Collaborative practice agreements between pharmacists and prescribers in Indiana may have a maximum term of two years, after which they must be reviewed and renewed. This timeframe ensures regular evaluation of patient care protocols.
Which condition allows a faxed Schedule II prescription to serve as the original in Indiana?
Patient is in a hospice program
Sent from a retail pharmacy
Outpatient clinic setting
When telephone verification is obtained
Indiana and federal regulations permit a faxed Schedule II prescription to serve as the original only if the patient is in a certified hospice program. The fax must clearly indicate the hospice status. Other faxed CII prescriptions still require a hard copy.
What does the 'X' prefix in a DEA number indicate?
New DEA registrant
Authorization to prescribe buprenorphine for opioid dependence
Veterinary prescriber
Hospital-based practitioner
An 'X' prefix in a DEA number designates that the practitioner is waivered to prescribe buprenorphine for opioid addiction treatment under the Drug Addiction Treatment Act (DATA 2000). This specialized registration expands access to medication-assisted therapy.
A pharmacy that distributes controlled substances to other registrants in excess of what percentage of its total controlled substance distribution must register as a distributor?
10%
1%
5%
20%
Federal law requires that a pharmacy register as a distributor if the total number of controlled substance dosage units distributed to practitioners or other pharmacies exceeds 5% of all controlled substances dispensed in a calendar year. This prevents diversion and maintains regulatory control.
When a pharmacy changes ownership in Indiana, within how many days must the new owner apply for a new license?
15 days
45 days
30 days
7 days
Indiana law requires the new owner of a pharmacy to submit an application for licensure within 30 days of ownership transfer. This ensures uninterrupted compliance and oversight by the Board.
Which security feature must be included on all prescription pads for controlled substances in Indiana?
Microprinting
Tamper-evident ink
Watermarked paper
Pad identification number
Indiana requires prescription pads for controlled substances to bear a unique pad identification number. This feature helps prevent unauthorized copying and prescription fraud. Prescribers must obtain new pads if numbers run out.
How often must automated record-keeping systems back up controlled substance transaction data under Indiana regulations?
Every 24 hours
Weekly
Hourly
Monthly
Indiana rules mandate that any automated system used to record controlled substance transactions perform backups at least every 24 hours. This daily backup protects data integrity and ensures audit readiness. Pharmacies must verify backup logs regularly.
What is the maximum pharmacist-to-technician ratio allowed in Indiana pharmacies?
1:6
1:4
1:3
1:5
Indiana law permits one pharmacist to supervise up to four registered pharmacy technicians simultaneously. This ratio balances workload and maintains patient safety. Exceeding this ratio violates state regulatory standards.
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Study Outcomes

  1. Understand Essential Indiana Pharmacy Law Terminology -

    Define and recall key legal terms such as legend drugs, controlled substances, and prescriber authority within the context of Indiana Pharmacy Law.

  2. Apply Prescription and Dispensing Requirements -

    Outline valid prescription components under Indiana statutes, including labeling, refill limits, and documentation requirements.

  3. Differentiate Between Federal and Indiana Pharmacy Regulations -

    Distinguish state-specific mandates from federal pharmacy law provisions to ensure accurate compliance in real-world and exam scenarios.

  4. Analyze Indiana MPJE Practice Scenarios -

    Work through free MPJE practice questions on prescription processing and drug definitions to sharpen analytical skills and boost exam confidence.

  5. Identify Proper Controlled Substance Protocols -

    Determine appropriate scheduling, security measures, and record-keeping procedures for controlled substances under Indiana law.

  6. Evaluate Legal Consequences of Noncompliance -

    Recognize potential penalties and corrective actions for violations of Indiana pharmacy regulations to reinforce risk management strategies.

Cheat Sheet

  1. Legend Drug Definitions -

    In Indiana pharmacy law, legend drugs are those that require a prescription by state and federal regulations (e.g., "Rx Only" under 21 CFR Part 201). Use mpje free practice questions to test your recall of which products fall into the legend category. A simple mnemonic is LEGEND = "Labeled, Enforced, Government-Endorsed, Necessary Drugs."

  2. Prescription Requirements -

    Under IC 25-26.2, a valid prescription must include patient name, prescriber details, drug name, strength, dosage form, directions, and prescriber's signature or electronic equivalent. Whether written, oral (promptly reduced to writing), or electronic, incomplete information can lead to refusal to fill. Practice with mpje sample questions free to master recognizing missing elements.

  3. Controlled Substance Scheduling -

    Indiana follows the federal Controlled Substances Act scheduling (Schedules I - V) and mirrors it in state statutes (IC 35-48-2). Schedule I substances have no accepted medical use, while Schedule V are lowest potential for abuse. Remember "C1 - Criminal, C5 - Common" as a quick way to differentiate highest vs. lowest abuse potential.

  4. Pharmacist Responsibilities & Scope -

    Per the Indiana Board of Pharmacy and indiana mpje guidelines, pharmacists must verify prescriptions, counsel patients, and maintain confidentiality. Always confirm questionable orders with the prescriber and document any therapeutic substitutions. Reviewing realistic Indiana Pharmacy Law scenarios in practice quizzes boosts confidence in handling these duties.

  5. Recordkeeping & Inventory -

    Indiana requires biennial controlled substance inventories and two-year retention of prescription records (IC 25-26.2). Schedule II documents must be kept separate; Schedules III - V can be filed together but flagged for easy retrieval. Test your knowledge with targeted mpje free practice questions on recordkeeping to ensure compliance.

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