Federal mpje graded a - Study guides, Class notes & Summaries

PA MPJE 2024 QUESTIONS AND ANSWERS GRADED A+ Generic drug companies can submit what two abbreviated drug applications? ANDA or 505(b)(2) application What is the key difference between an ANDA and 505(b)(2) application? Drugs submitted under ANDA must be bioequivalent and have same route of administration, strength, and formulation Drugs submitted under 505(b)(2) can have different strength or formulation What Act approved in March of 2020 includes OTC monograph reform? The CARES Ac...

TN MPJE Practice Questions and Answers Graded A+ To assist the Board of Pharmacy in enforcing pharmaceutical laws, the board must employ investigators who: Are pharmacists Pharmacy Tech, takes a call from a physician who is calling in a new prescription for a patient. Pharmacy Tech may receive the new prescription as long as he is: Certified Pharmacist has been asked by the Tennessee Board of Pharmacy's peer review committee to provide information regarding the competency of Phar...

Jurisprudence Exam 1 Graded A+ What is the MPJE? Multistate Pharmacy Jurisprudence Examination that combines federal and state specific questions How many attempts are there per jurisdiction for the MPJE? 5 attempts Brainpower Read More What is the waiting period after a failed MPJE attempt? 30 days What are the 4 competencies of the MPJE? 1: Licensure/personnel (22% of exam) 2: Pharmacist practice (33% of exam) 3: Dispensing requirements (24% of exam) 4: Pharmacy operations (21% of...

Florida MPJE Study Guide 2024 Seamon Already Graded A Sherman Antitrust Act This act: Outlaws agreements that restrain trade. Prevent monopolies and mergers that lessen competition Federal Food Drug and Cosmetic Act This act states: No adulterated or misbranded drugs in interstate commerce Adulteration Gross - Think inside the capsule Misbranded Improperly labeled - think outside the bottle FDCA This act requires: ingredients are disclosed on bottle drug must be proven safe before marketing...

Dr. C's MPJE: Chapter 2 Questions and Answers Graded A+ Which class of drugs is described below? High potential for abuse and severe potential for dependence (addiction); No currently accepted medical use in treatment in the US Schedule I (C1) drugs List examples of C-1 drugs. Opiates and derivatives such as heroin and dihydromorphine; hallucinogens such as marijuana, lysergic acid diethylamide (LSD), peyote, and mescaline; and depressants such as methaqualone Is marijuana legal in FL? Whil...

Federal MPJE Practice Questions Already Graded A+ A DEA Form 41 is used to document which of the following? on-site destruction of controlled substances A drug has an NDC of . The 0350 represents: the identity of the drug A drug manufacturer finds that bottles labeled "loratadine 10mg tablets" actually contain 5mg tablets, and issues a recall of the affected lot. Which of the following is true of this product? it is both adulterated and misbranded A manufacturer has a drug that i...

DEA 224 Registration for: - Retail pharmacies - Hospitals/clinics - Practitioners - Teaching Institution - Mid-Level Practitioners Retail pharmacy registration 224 Hospital registration 224 Clinic registration 224 Practitioner registration 224

NEVADA MPJE EXAM | QUESTIONS & ANSWERS (VERIFIED) | LATEST UPDATE | GRADED A+ Laws vs. Regulations Correct Answer: laws - enacted through a federal or state legislative process regulations - (or rules) provide specific details to help implement the law, and are issued by state regulatory agencies (e.g. state board of pharmacy) FDA Drug Approval Process Correct Answer: 1) pre-clinical testing (animals) 2) manufacturer files an investigational new drug (INDA) application with the FDA ...

TX MPJE LATEST UPDATE GRADED A+ Food Drug and Cosmetic Act of 1938 Followed deaths by sulfanalimide elixier; required new drugs to be SAFE; established FDA as primary federal law dealing with food, drug, costmetic, and medical device safety Durham-Humphrey Act of 1951 Established Rx and OTC drug class; authorized verbal prescriptions and prescription refills Kefauver-Harris Amendment of 1962 Required new drugs to be SAFE and EFFECTIVE; increased safety requirements for drugs and est...

DEA 224 Registration for: - Retail pharmacies - Hospitals/clinics - Practitioners - Teaching Institution - Mid-Level Practitioners Retail pharmacy registration 224 Hospital registration 224 Clinic registration 224 Practitioner registration 224