Focus On Generic Drugs

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africa: CONTESTED WTO COMPROMISE ON GENERIC DRUGS

A last-minute World Trade Organization compromise in Geneva on intellectual property protection and access to medicines is being heralded by some as finally opening the doors to imports of generic medicines by poor countries without a manufacturing capability. In intense negotiations in recent months, the U.S. reached behind-thescenes agreements with key countries such as Brazil, India, South A...

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Bioequivalence of generic drugs.

Generic drugs are bioequivalent to the original brand; this is a prerequisite for marketing approval. It is theoretically possible that one generic drug may overestimate the pharmacokinetic (PK) parameters of the original and another generic may underestimate these PK parameters; in consequence, these 2 generics may not be bioequivalent between themselves. The result could be loss of efficacy o...

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The concept of: Generic drugs and patented drugs vs. brand name drugs and non-proprietary (generic) name drugs

Time and again the importance of generic prescribing has been emphasized, primarily to reduce the cost of drugs (Mukherjee, 2013). There are two concepts to be understood here, one is generic vs. patented drugs and the other is a drug’s “brand name” vs. “non-proprietary name” or “generic name.” Although, our article primarily describes the Indian scenario, it can be extrapolated to other countr...

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Generic versus brand-name drugs

What?s in a name? A brand-name drug and its generic counterpart are chemically the same. They may have different names, colors, and shapes, but the United States Food and Drug Administration (FDA) requires generic drugs to share several similarities as the brand-name counterparts (more on this later). And, while there are some differences, generics don?t really change the effectiveness of the d...

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Generic versus brand-name drugs

What?s in a name? A brand-name drug and its generic counterpart are chemically the same. They may have different names, colors, and shapes, but the United States Food and Drug Administration (FDA) requires generic drugs to share several similarities as the brand-name counterparts (more on this later). And, while there are some differences, generics don?t really change the effectiveness of the d...

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ژورنال

عنوان ژورنال: Chemical & Engineering News Archive

سال: 2002

ISSN: 0009-2347,2157-4936

DOI: 10.1021/cen-v080n038.p005