Legend drugs Study guides, Class notes & Summaries

MPJE Maryland Exam (Latest 2023/ 2024 Update) Questions and Verified Answers | 100% Correct| Grade A Q: How long to retain CE credit records? Answer: 4 years Q: What actions can board take against registration? Answer: Suspend, deny, or revoke Q: What tasks can a technician perform? Answer: Fill script from stock bottle; reconstitute medication;initiate and receive refill authorization requests; prepare/package bulk prescriptions;load automated dispensing sys...

Administrative Procedure Act - correct answer federal law enacted in 1946, "notice and comment rulemaking" 1906: The Pure Food and Drug Act (PFDA) - correct answer interstate commerce labeling 1912 Pure Food and Drug Act - correct answer revised in 1912, stated that a drug was misbranded if its label contained a "false and fraudulent" statement regarding "curative or therapeutic effect." 1938 FD&C Act - correct answer • extended control to cosmetics and therapeutic de...

What is the 1938 Federal Food, Drug and Cosmetic Act? (Ans- Misbranding and mislabeling What is the 1951 Durham-Humphrey Amendment? (Ans- Distinction between legend drugs and otc drugs What is the 1970 Poison Prevention Packaging Act? (Ans- Made sure all manufacturers and pharmacies to place medications with childproof caps and packaging What is the 1983 Orphan Drug Act? (Ans- Encourages companies to develop drugs for rare diseases by providing research assistance, grants and co...

Federal MPJE (2024/2025) Exam Questions and Answers 100% Solved What did the FDCA of 1938 accomplish? Food, Drug, and Cosmetic Act Drugs must be safe prior to marketing Established the FDA - Food, Drug, Cosmetic, Medical device safety Durham-Humphrey Amendment of 1951 Created a distinction between "OTC" and "Legend Drugs/Prescription". Authorized verbal prescriptions/refills Required Legend Drugs to carry the statement: "Caution: Federal law prohibits dispensing without a presc...

North Dakota ND MPJE Questions and Answers 100% Pass How many members serve on the Board of Pharmacy? 7: 5 pharmacists, 1 registered technician, 1 public member How many are public members? (not pharmacist, no financial interest in the field, not spouse of RPh or someone who has financial interest in the field) 1 Which of the following can prescribe legend drugs: O.D. (Optometrist)- Nurse Practitioner - Clinical Nurse Specialist - Physician's Assistant - Midwife - Nurse Midw...

Penn Foster Pharmacology Proctor Exam(Answered 100% Correctly) Indications reasons for giving a drug contraindications reasons to not give a drug legend drugs drugs that have the ability to cause serious harm if misused, must be regulated by the FDA as prescription drugs. Contain a caution statement "caution federal law restricts the use of this drug to use/by/or on the order of a licensed veterinarian." veterinarian client relationship vet takes responsibility for making decisio...

(Updated) EXCPT Pharmacy Technician Exam Study Guide with complete solutions |Latest 2024/2025 1. Pure Food and Drug Act (1906) Prohibits interstate commerce of misbranded and adulterated drugs and foods. 2. Misbranded a drug product is misbranded if its labeling is inaccurate, incomplete, or misleading 3. Adulterated a drug product that fails to meet quality, strength, or purity standards 4. Federal Food, Drug, and CosRequires drug manufacturers to provide the FDA with evidence of saf...

Schedule I Legend drugs requires rx schedule IA Drugs on CPP, must be on duplicate prescription Schedule II Professional Service Area- BTC - NPA Schedule III Professional Products Area- Drugs can be sold to anyone OTC area of licensed pharmacy Schedule IV Prescription by pharmacist, drugs that can be prescribed by a pharmacist Unscheduled Non pharmacy sale, drugs may be sold by non pharmacist to anyone The Health Professions Act-Through the Act, the Ministry of Health (MOA) delegates Auth...

What are the Alabama restrictions on the sale of ephedrine or pseudoephedrine containing products? - correct answer These products must be sold by a pharmacy licensed by ALBOP from behind the counter and a person may purchase no more than 3.6 grams per calendar day AND No more than 7.5 grams per 30 days (AL law). Purchaser must be at LEAST 18 years of age and Provide a valid, unsuspended driver's license or non-driver ID card issued by one of the 50 states, a U.S. Uniformed S...

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...