CNPR EXAM 2 ACTUAL TEST PAPER QUESTIONS CORRECT ANSWERS GRADED A PLUS
CNPR EXAM 2 2026/2027 Questions and Answers
Verified Solutions Latest Update
Question:
Answer:
Indications and usage ✔✔What must drugs labels include? - ✔✔Indications, usage and
contraindications ✔✔What should be in the description section of a drug's package insert
information? - ✔✔the drug's proprietary name and established name ✔✔Exclusivity gives
exclusive ______, is granted by the FDA, and can run concurrently with a patent or not. -
✔✔Marketing rights ✔✔What differentiates exclusivity from a patent? - ✔✔Exclusivity is only
granted upon the drug's FDA approval ✔✔What is required of an invention for it to be worthy of
patent protection? - ✔✔It must be novel, useful, and not obvious ✔✔A generic drug is _____ to the
originator brand-name drug in dosage, strength, safety and quality. - ✔✔Bio-equivalent ✔✔What is
not a requirement by the FDA's criteria for Equivalency? - ✔✔That the drugs contain identical
amounts of the same inactive ingredients ✔✔Approved Drug Products with Therapeutic
Equivalence - ✔✔the most reliable source of information on therapeutically equivalent drug
products. ✔✔What is the term for chemical equivalents which, when administered in the same
amounts, will provide the same biological or physiological availability as measured by blood and
urine levels? - ✔✔Biological equivalents ✔✔Generic Substitution - ✔✔The dispensing of an
unbranded generic product for the product prescribed? ✔✔What is the duration of a patent
challenge? - ✔✔180 days ✔✔Drug sample closet - ✔✔The more visibility you can give your drug,
the more likely it will be prescribed ✔✔Pharm reps typically store and secure their own samples -
✔✔True ✔✔Sampling is sometimes the most important factor in a pharmaceutical rep's success
Question:
Answer:
True ✔✔Who approves the storage conditions for a drug? - ✔✔The FDA ✔✔Pharm reps must
always record the amount of drug samples left and obtain a signature for the amount. - ✔✔True
✔✔What is prohibited by Section 503 of the Federal Food, Drug and Cosmetic Act, as amended by
the Prescription Drug Act? - ✔✔The sale, purchase, trade or offer to sell, purchase or trade
prescription drug samples. ✔✔Who regulates the drug sampling for a Pharm rep? - ✔✔The FDA
✔✔United States Pharmacopoeial Convention - ✔✔Issues monographs that define how drugs
CNPR EXAM 2 2026/2027 Questions and Answers
Verified Solutions Latest Update
Question:
Answer:
Indications and usage ✔✔What must drugs labels include? - ✔✔Indications, usage and
contraindications ✔✔What should be in the description section of a drug's package insert
information? - ✔✔the drug's proprietary name and established name ✔✔Exclusivity gives
exclusive ______, is granted by the FDA, and can run concurrently with a patent or not. -
✔✔Marketing rights ✔✔What differentiates exclusivity from a patent? - ✔✔Exclusivity is only
granted upon the drug's FDA approval ✔✔What is required of an invention for it to be worthy of
patent protection? - ✔✔It must be novel, useful, and not obvious ✔✔A generic drug is _____ to the
originator brand-name drug in dosage, strength, safety and quality. - ✔✔Bio-equivalent ✔✔What is
not a requirement by the FDA's criteria for Equivalency? - ✔✔That the drugs contain identical
amounts of the same inactive ingredients ✔✔Approved Drug Products with Therapeutic
Equivalence - ✔✔the most reliable source of information on therapeutically equivalent drug
products. ✔✔What is the term for chemical equivalents which, when administered in the same
amounts, will provide the same biological or physiological availability as measured by blood and
urine levels? - ✔✔Biological equivalents ✔✔Generic Substitution - ✔✔The dispensing of an
unbranded generic product for the product prescribed? ✔✔What is the duration of a patent
challenge? - ✔✔180 days ✔✔Drug sample closet - ✔✔The more visibility you can give your drug,
the more likely it will be prescribed ✔✔Pharm reps typically store and secure their own samples -
✔✔True ✔✔Sampling is sometimes the most important factor in a pharmaceutical rep's success
Question:
Answer:
True ✔✔Who approves the storage conditions for a drug? - ✔✔The FDA ✔✔Pharm reps must
always record the amount of drug samples left and obtain a signature for the amount. - ✔✔True
✔✔What is prohibited by Section 503 of the Federal Food, Drug and Cosmetic Act, as amended by
the Prescription Drug Act? - ✔✔The sale, purchase, trade or offer to sell, purchase or trade
prescription drug samples. ✔✔Who regulates the drug sampling for a Pharm rep? - ✔✔The FDA
✔✔United States Pharmacopoeial Convention - ✔✔Issues monographs that define how drugs
