CDR DTR Practice Exam: 100% Verified Questions &
Answers: A+ Guide Solution
/.Prescription drugs can be purchased by a properly licensed entity using which of the
following methods? - Answer-A) Cash
B) Credit Card
C) Check
D) All of the above
E) Only B & C can be used.*
/.It is a violation of the Florida Law if a Transaction history, information and statement
(T3) for a prescription drug is NOT received under the following conditions? - Answer-A)
With or prior to the shipment of prescription drugs products.
B) For all prescription and over the counter drugs
C) From all prescription drug product manufacturers and wholesalers
D) Only A & C are correct*
E) All of the above
/.It is a prohibited act for a permitted establishment to do which of the following? -
Answer-A) Constructively refusing the department to enter or inspect an establishment
where drugs are held.
B) Refusal to allow the department to take samples of any drug.
C) Refusal to allow the department to inspect any vehicle used to transport drugs.
D) Purchasing or sale of a prescription drug in exchange for currency.
E) All of the above.*
/.A Florida licensed prescription drug wholesale distributor commits a
________________ if they knowingly traffic in over $25,000 in contraband precription
drugs? - Answer-A) A first degree felony*
B) A second degree misdemeanor
C) A third degree felony
D) A regulatory violation
/.Failure to deliver a complete and accurate transaction history, information and
statement at the time of distribution of a prescription drug makes the prescription drug a
________________ product. - Answer-A) Mislabeled
B) Counterfeit
C) Misbranded
D) Contraband*
, /.Refusal or constructve refusal to allow inspection of a facility that is suspected to hold
drugs, devices or cosmetics could classified as what type of violation? - Answer-A)
Criminal Felony
B) Regulatory Compliance Violation
C) Neither A or B
D) Both A and B*
/.Trafficking in contraband prescription drugs is defined as a person who knowingly
sells, purchases, manufactures, delivers, or brings into this State any amount of
contraband drug worth in excess of $____________. - Answer-A) $5,000.00
B) $10,000.00
C) $15,000.00
D) $20,000.00
E) $25,000.00*
/.In determining if a drug registration application is complete the Department can review
the following: - Answer-A) The Federal, Food, Drug and Cosmetic Act to assure the
product also complies with this Act.
B) Catalogs and labeling for the Product
C) Nothing is required other than the application if the products are already registered
with the FDA.
D) DESI listing and other literature as needed.
E) A, B and D all include required review items*
/.A repackaged prescription drug must follow the rules of the Federal Act and must
include all of the following on the label. - Answer-A) Name of drug, strength, dosage
form and expiration of the drug.
B) Name of drug, strength and expiration date of drug.
C) Manufacturer's name and lot #, name of drug, dosage form, strength and expiration
of the drug.*
D) Maufacturer's name and lot #, name of drug, strength and dosage form of the drug.
/.Any person who manufactures, packages, repackages, labels or relabels a drug in this
State must register such drug annually with the department. - Answer-True
False*
/.A Florida product registration for prescription drugs must be renewed how often? -
Answer-A) Biennially
B) Every 2 years
C) Annually
D) Biannually
E) A & B are correct*
/.A prescription drug for which the required Transaction history, information or statement
is missing or incomplete is considered: - Answer-A) Adulterated
B) Misbranded
Answers: A+ Guide Solution
/.Prescription drugs can be purchased by a properly licensed entity using which of the
following methods? - Answer-A) Cash
B) Credit Card
C) Check
D) All of the above
E) Only B & C can be used.*
/.It is a violation of the Florida Law if a Transaction history, information and statement
(T3) for a prescription drug is NOT received under the following conditions? - Answer-A)
With or prior to the shipment of prescription drugs products.
B) For all prescription and over the counter drugs
C) From all prescription drug product manufacturers and wholesalers
D) Only A & C are correct*
E) All of the above
/.It is a prohibited act for a permitted establishment to do which of the following? -
Answer-A) Constructively refusing the department to enter or inspect an establishment
where drugs are held.
B) Refusal to allow the department to take samples of any drug.
C) Refusal to allow the department to inspect any vehicle used to transport drugs.
D) Purchasing or sale of a prescription drug in exchange for currency.
E) All of the above.*
/.A Florida licensed prescription drug wholesale distributor commits a
________________ if they knowingly traffic in over $25,000 in contraband precription
drugs? - Answer-A) A first degree felony*
B) A second degree misdemeanor
C) A third degree felony
D) A regulatory violation
/.Failure to deliver a complete and accurate transaction history, information and
statement at the time of distribution of a prescription drug makes the prescription drug a
________________ product. - Answer-A) Mislabeled
B) Counterfeit
C) Misbranded
D) Contraband*
, /.Refusal or constructve refusal to allow inspection of a facility that is suspected to hold
drugs, devices or cosmetics could classified as what type of violation? - Answer-A)
Criminal Felony
B) Regulatory Compliance Violation
C) Neither A or B
D) Both A and B*
/.Trafficking in contraband prescription drugs is defined as a person who knowingly
sells, purchases, manufactures, delivers, or brings into this State any amount of
contraband drug worth in excess of $____________. - Answer-A) $5,000.00
B) $10,000.00
C) $15,000.00
D) $20,000.00
E) $25,000.00*
/.In determining if a drug registration application is complete the Department can review
the following: - Answer-A) The Federal, Food, Drug and Cosmetic Act to assure the
product also complies with this Act.
B) Catalogs and labeling for the Product
C) Nothing is required other than the application if the products are already registered
with the FDA.
D) DESI listing and other literature as needed.
E) A, B and D all include required review items*
/.A repackaged prescription drug must follow the rules of the Federal Act and must
include all of the following on the label. - Answer-A) Name of drug, strength, dosage
form and expiration of the drug.
B) Name of drug, strength and expiration date of drug.
C) Manufacturer's name and lot #, name of drug, dosage form, strength and expiration
of the drug.*
D) Maufacturer's name and lot #, name of drug, strength and dosage form of the drug.
/.Any person who manufactures, packages, repackages, labels or relabels a drug in this
State must register such drug annually with the department. - Answer-True
False*
/.A Florida product registration for prescription drugs must be renewed how often? -
Answer-A) Biennially
B) Every 2 years
C) Annually
D) Biannually
E) A & B are correct*
/.A prescription drug for which the required Transaction history, information or statement
is missing or incomplete is considered: - Answer-A) Adulterated
B) Misbranded
