Pure food and drug act - Study guides, Class notes & Summaries

What legistation was created for the provisions for the fast track review of some NDA submissions to expedite approval of new drugs used to treat life-threatening conditions? - Food and Drug A dministration (FDA) Modernization Act 1997 What legistation encouraged manufacturers to conduct research for new uses of drugs and to submit SNDAs for these uses? - FDA modernization act 1997 What act reduced the cose of orphan drugs? - Orphan drug act 1983 What act prohibited the adulteration or misbrandi...

Test Bank on the Core Concepts in Pharmacology 5th Edition by Holland, Adams and Brice Table of Contents Chapter 1 ......................................................................................................................................... 3 Chapter 2 ....................................................................................................................................... 12 Chapter 3 ........................................................................................

TEST BANK Pharmacology Clear and Simple: A Guide to Drug Classifications and Dosage Calculations Cynthia J. Watkins 4th Edition Chapter 1. History of Pharmacology MULTIPLE CHOICE 1. The Greek word pharmakon means which of the following? a. Medicine b. Poison c. Remedy d. Medicine, poison, and remedy ANS: D Rationale: The word pharmakon refers to the curing of illness, thus meaning medicine and remedy, as well as poison because early medicines we...

NH MPJE Questions and Answers 100% Correct| Scored A+ 30 days ____ after the expiration date stated on the label of a drug stock container, becomes an adulterated drug Within 15 days Must notify the Board in writing of any changes in name, address or employment Within 15 days Prior to closing, must notify Board and regional office of DEA in writing of the intended closing of a pharmacy Within 30 days Any theft or loss of controlled substances must be reported on DEA for...

Multistate Pharmacy Jurisprudence(MPJE) Exam Review 2023 (FEDERAL LAW) Questions and Answers. Food and Drug Administration Correct Answer: a federal agency in the Department of Health and Human Services established to regulate the release of new foods and health-related products (P)FDA Correct Answer: Pure Food and Drug Act of 1906 Federal Food, Drug, and Cosmetic Act of 1938 (6/25/38) Correct Answer: FDCA Poison Prevention Packaging Act of 1970 Correct Answer: PPPA Controlled Substance of...

PTCB EXAM TEST BANK QUESTIONS AND ANSWERS LATEST WITH RATIONALE Multiple choice What is the route of administration for a prescription with the following directions: "i supp pr q 6 hr prn"? A. Orally B. Rectally C. Urethrally D. Vaginall {{Correct Ans- B. Rectally Rationale: "pr" means per rectum. What is the meaning of PDA? A. Personal digital aid B. Personal digital assistant C. Physician digital assistant D. Pharmaceutical data assistant {{Correct Ans- B. Personal dig...

Pure Food And Drug Act – Complete Guide

What are drug standards? - ANSWER rules that drug manufactures must follow when they produce drugs 1906 Pure Food and Drug Act - ANSWER est. drug standards for strength, purity, and quality. also mandated that drugs with with dangerous ingredients be labeled as such 1938 Federal Food, Drug, and Cosmetic Act - ANSWER established the Food and Drug Administration (FDA), which is meant to enforce rules such as labeling, drug approval before release, and warning labels

Drug Standards - ANSWER rules set to assure that consumers get what they pay for, that all preparations by the same drug name must be of uniform strength, quality, and purity 1906 Pure Food and Drug Act - ANSWER Prohibits the sale and transport of adulterated or mislabeled food, drinks and drugs. Prohibits the mislabeling and misbranding of products. 1938 Food, Drug, and Cosmetic Act - ANSWER created to enforce rules such as labeling, drug approval before release, and warning labels (such...

Pure Food and Drug Act (1906) aka Wiley Law - correct answer Prohibits adulteration and misbranding Food, Drug and Cosmetic Act (1938) - correct answer -New drug could not be marketed unless safe -Required manufacturer label to have directions for use and warnings about habit forming drugs Durham-Humphrey Amendment (1951) - correct answer -Established prescription and OTC drug categories -Allowed for oral prescriptions -Allowed for refills Manufacturer label on Rx drugs after Durham-...