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G is a list of frequently asked questions concerning generic medication: A generic drug is one which is identified by its official chemical name rather than an advertised brand name. The term has also come to mean a drug that has been introduced onto the market, usually after the patent on the brand-name drug has expired, through an approval process known as an Abbreviated New Drug Application (ANDA). Generics available in the U.S. have the same active chemical composition and have been demonstrated bioequivalent, i.e., deemed by the Food and & Drug Administration (FDA) to produce the same effect on the body as their brand-name counterparts. The following frequently asked questions and answers will help you better understand the benefits of generic drugs. Is there a difference in ingredients between a generic and a brand-name product? The active ingredients in the brand-name and generic products are the same. Both the brand-name and the generic versions must have the same potency, be available in the same dosage forms (i.e. tablet, liquid, injectable), be demonstrated safe and effective, and be manufactured under government-approved Good Manufacturing Practices (GMP). Significant differences in any of these areas would mean the generic drug would not be approved by the FDA, and therefore would not be available. Although the inactive ingredients such as fillers and dyes are allowed to be different, these ingredients should not affect the safety or efficacy of a drug in any way. In fact, brand-name as well as generic companies often change these inactive ingredients...with FD
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