Food and Drug Administration website

China s State Food and Drug Administration website, http //www.sfda.gov.cn/eng/. 

The list of drugs to be discontinued is continuously updated at the US Food and Drug Administration website, 2004,... 

FDA—Food and Drug Administration website concerning Color Additives ... 

Fortunately, for those that require information and a high level of detail in this area there is usually a comprehensive list of the applicable up-to-date regulations, and available guidance documents, on the national, European Union (EU) and US Food and Drug Administration websites. 

Approved quinolones as of February 2006 Generic available Marketed in the United States by Oscient. Source. U.S. Food and Drug Administration (FDA) website www.fda.gov/cder... 

State Food and Drug Administration of the People s Republic of China (2006) Technical guiding principles for the reproductive toxicity of drugs. SEDA website http //www.sfda.gov.cn/. Accessed 30 Jan 2012... 

US Food and Drug Administration Center for Drug Evaluation and Research. Office of Nonprescription Products website http //www.fda.gov/cder/offices/otc/default.htm... 

Pharmaceutical nonactive excipients have long been applied in a variety of pharmaceutical dosage forms to provide a wide range of functional characteristics that facilitate the optimal delivery of a drug to achieve the desired therapeutic effects. Pharmaceutical excipients are inert materials with no adverse effects on the safety and efficacy of therapeutic products. The Food and Drug Administration (FDA) website (1) provides a database listing all the FDA-approved nonactive pharmaceutical excipients. This provides formulation scientists a useful reference for efficient choices of the suitable excipients for the desired formulations of drug. 

Office of Regulatory Affairs, Food and Drug Administration Guide to Inspection of Pharmaceutical Quality Control Laboratories, July 1993 Website http //www.fda.gov/ora/inspect ref/igs/pharm.html. 

National Archives and Records Administration, Code of Federal Regulations, Title 21, Food and Drugs, Food and Drug Administration, Department of Flealth and Fluman Services, Part 320, Bioavailability and Bioequivalence Requirements. Website located at http //www.access. gpo.gov/cgi-bin/cfrassemble.cgi title= 199921. 

The Redbook 2000 provides guidance for the safety of food ingredients, and is produced by the US Food and Drug Administration (FDA), Center for Food Safety and Applied Nutrition (CFSAN). The first part of this guidance was issued in July 2000. It is available electronically at the website listed at the end of the article. 

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