July 2011
Beginner
446 pages
9h 36m
English
Content preview from An Introduction to Pharmaceutical Sciences
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3
Drugs, medicines, and regulatory authorities
Learning objective
This chapter looks at the common terms used for drugs – medicines, brand names, generic names, chemical names, prescription drugs and over-the-counter drugs – and at how drugs are developed. It describes how regulatory agencies regulate the quality of generic drugs and the role of pharmacopoeias (Figure 3.1).
Figure 3.1 The talking points of Chapter 3
Key concept terms
Bioequivalency
in-vivo equivalency between brand name and generic name drugs regarding pharmacokinetic profiles
Blockbuster drug
a drug whose annual sale is US$1 billion or more
Brand name
trade or proprietary ...
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