Texas MPJE Exam February 2024/2025 (Study Guide based off
Dr. C's Ultimate Texas MPJE Review 2024) Actual Complete Real
Exam Questions & Answers.
Discuss what constitutes as "unprofessional conduct" -
ANSWER-"unprofessional conduct" is defined as engaging in
behavior or committing an act that fails to conform with the
standards of the pharmacy profession, including, but not limited
to criminal activity or activity involving moral turpitude,
dishonesty, or corruption.
-dispensing fraudulent prescription
-delivering prescriptions
-sharing compensation w/ practitioner that was received from an
individual who received pharmacy services
-refusing inspection
-Subverting or attempting to subvert NAPLEX/MPJE
-failing to practice pharmacy in an acceptable manner
-Obstructing a board member from performing their duties
-Intimidating/threatening a board member
-failing to maintain controls to prevent diversion
-dispensing RX while not acting in usual course of pharmacy
practice
-failing to correct issues identified by a warning notice
,A pharmacy must report to the Texas State Board of Pharmacy
within___ days after the permanent closing of a pharmacy. -
ANSWER-10 Days after closing
What is a Class D pharmacy? - ANSWER-Clinic pharmacy
A facility/location other than a physician's office, where limited
types of noncontrolled drugs or devices restricted to the clinic's
formulary are stored, administered, provided, or dispensed to
outpatients (i.e., Planned Parenthood)
The formulary for a Class D pharmacy (Clinic pharmacy) shall not
contain the following drugs:
291.93 (e)(1)(C) - ANSWER-FORMULARY SHALL NOT CONTAIN:
*Nalbuphine (Nubain) - injectable opioid analgesic
*Erectile dysfunction drugs
*Schedule II-V substances
What is a Class E pharmacy? - ANSWER-Non-resident pharmacy
(not located in Texas) whose primary business is to dispense a
prescription, drug, or device under a prescription drug order and
deliver the drug or device to patients in Texas.
,What is a Class F pharmacy? - ANSWER-Freestanding Emergency
Medical Care Facilities (FEMCF)
A freestanding facility that is licensed by the Texas Department of
State Health Services to provide emergency care to patients.
Sales of pseudoephedrine-containing products to an individual in
Texas are limited to ____ grams per day and____ grams per 30
days. - ANSWER-3.6 grams per day and 9 grams per 30 days
FDA Orange Book uses two letter code system: - ANSWER-First
letter is key,
A= drug products that FDA considers pharmaceutically and
therapeutically equivalent
B= drug products that FDA considers NOT pharmaceutically and
therapeutically equivalent
AB= products with actual or potential bioequivalence problems,
but for which adequate scientific data has established
bioequivalence
, FDA Orange Book: When there are multiple pharmaceutically
equivalent reference drugs that have not been determined to be
bioequivalent the FDA implemented: - ANSWER-a three character
code (AB1, AB2, AB3 etc)
If a generic drug establishes bioequivalence with one of the
reference drugs it will receive the same three letter code
FDA Orange Book: Products with no known or suspected
bioequivalence issues...(AA, AN, AO, AP, AT) - ANSWER-AA=
conventional dosage forms
AN= solutions/powders for aerosolization
AO= injectable oil solutions
AP= injectable aqueous solutions
AT= topical products
Scheduling authority for controlled substances (federal versus
texas state) -
ANSWER-Federal= US Attorney General
Texas= The Commissioner of Texas Department of State Health
Services
A pharmacy may compound narcotics pursuant to a prescription;
however, DEA limits the compounding of aqueous or oleaginous
Dr. C's Ultimate Texas MPJE Review 2024) Actual Complete Real
Exam Questions & Answers.
Discuss what constitutes as "unprofessional conduct" -
ANSWER-"unprofessional conduct" is defined as engaging in
behavior or committing an act that fails to conform with the
standards of the pharmacy profession, including, but not limited
to criminal activity or activity involving moral turpitude,
dishonesty, or corruption.
-dispensing fraudulent prescription
-delivering prescriptions
-sharing compensation w/ practitioner that was received from an
individual who received pharmacy services
-refusing inspection
-Subverting or attempting to subvert NAPLEX/MPJE
-failing to practice pharmacy in an acceptable manner
-Obstructing a board member from performing their duties
-Intimidating/threatening a board member
-failing to maintain controls to prevent diversion
-dispensing RX while not acting in usual course of pharmacy
practice
-failing to correct issues identified by a warning notice
,A pharmacy must report to the Texas State Board of Pharmacy
within___ days after the permanent closing of a pharmacy. -
ANSWER-10 Days after closing
What is a Class D pharmacy? - ANSWER-Clinic pharmacy
A facility/location other than a physician's office, where limited
types of noncontrolled drugs or devices restricted to the clinic's
formulary are stored, administered, provided, or dispensed to
outpatients (i.e., Planned Parenthood)
The formulary for a Class D pharmacy (Clinic pharmacy) shall not
contain the following drugs:
291.93 (e)(1)(C) - ANSWER-FORMULARY SHALL NOT CONTAIN:
*Nalbuphine (Nubain) - injectable opioid analgesic
*Erectile dysfunction drugs
*Schedule II-V substances
What is a Class E pharmacy? - ANSWER-Non-resident pharmacy
(not located in Texas) whose primary business is to dispense a
prescription, drug, or device under a prescription drug order and
deliver the drug or device to patients in Texas.
,What is a Class F pharmacy? - ANSWER-Freestanding Emergency
Medical Care Facilities (FEMCF)
A freestanding facility that is licensed by the Texas Department of
State Health Services to provide emergency care to patients.
Sales of pseudoephedrine-containing products to an individual in
Texas are limited to ____ grams per day and____ grams per 30
days. - ANSWER-3.6 grams per day and 9 grams per 30 days
FDA Orange Book uses two letter code system: - ANSWER-First
letter is key,
A= drug products that FDA considers pharmaceutically and
therapeutically equivalent
B= drug products that FDA considers NOT pharmaceutically and
therapeutically equivalent
AB= products with actual or potential bioequivalence problems,
but for which adequate scientific data has established
bioequivalence
, FDA Orange Book: When there are multiple pharmaceutically
equivalent reference drugs that have not been determined to be
bioequivalent the FDA implemented: - ANSWER-a three character
code (AB1, AB2, AB3 etc)
If a generic drug establishes bioequivalence with one of the
reference drugs it will receive the same three letter code
FDA Orange Book: Products with no known or suspected
bioequivalence issues...(AA, AN, AO, AP, AT) - ANSWER-AA=
conventional dosage forms
AN= solutions/powders for aerosolization
AO= injectable oil solutions
AP= injectable aqueous solutions
AT= topical products
Scheduling authority for controlled substances (federal versus
texas state) -
ANSWER-Federal= US Attorney General
Texas= The Commissioner of Texas Department of State Health
Services
A pharmacy may compound narcotics pursuant to a prescription;
however, DEA limits the compounding of aqueous or oleaginous
