Connecticut MPJE Final Exam 2025- Updated -
100% Verified Questions + In-Depth Explanations
Questions and Mark scheme
Version: Final 1.1
,What components must a label have to be considered NOT MISBRANDED - ✔✔Drug name
Drug strength
Lot number
Manufactuer
date of exipiration
What must be on the label of a generically subsititued drug - ✔✔Drug dispensed, if not brand, must have generic +
manufactuer name
unless a prescriber says no in writing orally or by electronic means.
What must the record of a substituted prescription have - ✔✔brand name of drug substituted or if not brand, generic
name and manufacturer
retail price of substituted drug at time of dispensing.
What must a pharmacist do to dispense an epipleptic brand - ✔✔Pharmacist must notify both patient and prescriber
Get written consent of prescriber
T/F A pharmacist can substitute a different dosage form; oral tablet or liquid - ✔✔True
A pharmacist can substitute a dosage form if? - ✔✔The doctor is not readily available for consultation
If the original form does not have special release technology
The form dispensed has the same strength dose and dose schedule.
Who does a pharmacist need to inform of dosage form substitution - ✔✔Patient and prescriber at earliest reasonable
time
What is the definition of AB rated products - ✔✔Product meets necessary bioequivalance requirements and may be
substituted if equivalancy problem resolved by in vivo/and or in vitro studies
T/F a hospital ED can dispense a contorl medication - ✔✔False
,When can a HOSPITAL ED dispense a medication - ✔✔Therapeutic needs of patient require that medication be initiated
immediately
24 hour supply only
Services of a licensed pharmacy are not avialble within a 5 mile radius
What are the responisbilities of a pharmacists/ - ✔✔Guard against prescription fraud
be aware of type of fradulent Rxs
Learn Prevention techniques
Implement proper controls
A photo ID is required for everyone who is unknown to a pharmacist who is purchasing a control - ✔✔YES
When is a photo ID not required for a control substance - ✔✔Institutional setting
What are the drugs covered by the CSA - ✔✔Hallucinogens
narcotics
amphetamine
barbiturates
tranquilizers
anabolic steroids
An RPH is permitted to compound aqueous, oleaoginous or solid dosage form up to what percent of C2-c5 DRUGS -
✔✔20%
What are the DEA FORMS 225/225a for - ✔✔Manufactuer
Distributor
Reverse Distributor
Researcher
Analytical Laboratory
Importer
Exporter
, What DEA forms 363/363a - ✔✔Narcotic Treatment Program
What are the DEA forms 224/224a - ✔✔Retail pharmacy/Central fill pharmacy
hospital/clonic
practitioner
Teaching institution
What are the 5 available methods for disposal from practitioner registrant's inventory - ✔✔On site method
Reverse Distributor
Return or Recall (If CII, USE DEA form 222)
DEA request for assistance (DEA Form 41)
If reguarly disposing CS, by single request to DEA with condition
What methods can practictioners only use if they are collector - ✔✔REVERSE distributo
On site method
DEA form 41
How many witnesses does it involve for disposal of Controlled substances - ✔✔2
What are examples of C2 drugs - ✔✔Cocaine, amobarbital, glutehimide, pentobarbital.
Desoxyn(methamphetamine)
Methadone Maintenance & Detox must be done under SEPARATE dea registration as a narcotic treatment program -
✔✔True
In order for program for Methadone & Maintenance to be approved who must approve it - ✔✔Center for Substance
Abuse Treatment
What are examples of C3 schedule drugs - ✔✔Benzphetamine(Didrex), phendimetrazine, ketamine
Oxadrolone(Oxandrin)
amobarbital, secobarbital, pentobarbital and dronabinol (Marinol)