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...d Drug Administration (United States)|U.S. Food and Drug Administration]] (FDA). It was approved June 21, 1996 for adults and September 11, 1998 for child ...http://www.fda.gov/medwatch/safety/2000/viramune.htm Viramune (nevirapine) letter (November 2000)]</ref> Unacceptably high risk of serious liver symptoms in

...States)|Food and Drug Administration]] (FDA) in 1987. Ciprofloxacin has 12 FDA-approved human uses and other veterinary uses, but it is often used for non ...Bayer introduced ciprofloxacin in 1987 and was later approved by the U.S. FDA on 22 October 22 1987 for use in the United States to treat specific bacter

...armaceuticalCompanies/UCM165406.pdf Food and Drug Administration: Anvirzel Letter, dated March 7, 2000. Retrieved on 2009-07-27.<!-- Bot generated title -->]

...shed Rose's warning letter on his blog.{{ref label|Yahoo|10|^}}{{ref label|letter|11|^}}{{ref label|PH|12|^}} ...ww.defendingscience.org/case_studies/upload/National_Jewish_FDA_Letter.pdf Letter from Cecile Rose to U.S. Food and Drug Administration], from ''www.defendin

...rmined that the substance was a drug rather than a supplement and issued a warning,<ref>{{Cite news | title = FDA warns maker of product used as alternative autism treatment

...tates before being voluntarily withdrawn from the market after a July 2005 FDA advisory warned of a high overdose potential when taken with alcohol. As of ..., 2010. Because of federal government closings during snow conditions, the FDA briefly extended the approval date to March 1, 2010.

....gov/drugsatfda_docs/appletter/2005/021196s005ltr.pdf |title= FDA Approval Letter for Xyrem; Indication: EDS (Excessive Daytime Sleepiness) associated with n ...ts to submit a New Drug Application to the US Federal Drug Administration (FDA) before the end of 2009 for JZP-6, for use in treating Fibromyalgia.