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Florida Cdr Final Exams Actual Questions And Answers Sure

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FLORIDA CDR FINAL EXAMS ACTUAL QUESTIONS AND ANSWERS SURE

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FLORIDA CDR FINAL EXAMS ACTUAL QUESTIONS
AND ANSWERS SURE A+
✔✔Does a T3 apply to a medical convenience kit? - ✔✔No, it is exempt

✔✔A medical Convenience kit - ✔✔Means packages or units that contain combination
products

✔✔A medical convenience kit contains controlled substances. True or false - ✔✔False

✔✔It is a violation of the Florida law if a transaction history, information in statement
(T3)for a prescription drug is not received under the following conditions? - ✔✔With or
Prior to the shipment of prescription drug products and from all prescription drug
product manufacturers in wholesalers.

✔✔It is prohibited act for permitted establishment to do which of the following -
✔✔Constructively Refusing the department to enter or inspect and establishment where
drugs or hell, refusal to allow the department to take samples of a drug, refusal to allow
the department to inspect any vehicle used to transport drugs and purchasing or selling
prescription drugs in exchange for currency.

, ✔✔A Florida license prescription drug wholesale distributor commits a _________ if
they know any traffic in over $25,000 in contraband - ✔✔A first-degree felony

✔✔Refusal or constructive refusal to allow inspection of a facility that is suspected to
hold drugs, devices or cosmetics can be classified as what type of violation? - ✔✔

✔✔Trafficking in contraband prescription drugs is defined as a person who knowingly
sells, purchases, manufacturers, delivers, or brings into the state any amount of
contraband worth in excess of $_____________ - ✔✔$25,000

✔✔Trafficking in contraband prescription drugs in the state of Florida is a_________? -
✔✔First-degree felony

✔✔What does FDA stand for? - ✔✔United States food and drug administration

✔✔In determining if a drug registration application is complete the department can
review the following : - ✔✔The federal, food drug and cosmetic act to assure the
product also Complies with the act, catalogs and labeling of the product, DESI listing
and other literature as needed

✔✔What are the labeling requirements for prescription drugs? - ✔✔Drug name,
strength, dosage, manufactures name, lot number, expiration date, must be on the
label. NDC is not required

✔✔Any person who manufactures, packages, three packages, labels or relabels a drug
in the state must register such drug annually with the department. True or false -
✔✔False

✔✔A repackage prescription drug must follow the rules of the federal act and must
include all of the following on the label : - ✔✔Manufactures name and lot number, name
of drug, dosage form, strength and expiration of the drug

✔✔A Florida product record registration for prescription drugs must be renewed how
often? - ✔✔Biennially, every two years

✔✔A prescription drug for which they require transaction history, information or
statement is missing or incomplete is considered : - ✔✔Adulterated and contraband

✔✔If a prescription drug is expired it is considered to be : - ✔✔Adulterated

✔✔A drug is considered adulterated if the strength, quantity and or purity falls below
that of which is in the official compendium (USP). True or false - ✔✔True

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