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...rchType=BasicSearch&Search_Button=Submit&searchTerm=076747 Drugs@FDA]. U S Food and Drug Administration</ref> ...rchType=BasicSearch&Search_Button=Submit&searchTerm=076798 Drugs@FDA]. U S Food and Drug Administration</ref>

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...rchType=BasicSearch&Search_Button=Submit&searchTerm=020733 Drugs@FDA]. U S Food and Drug Administration</ref> ...rchType=BasicSearch&Search_Button=Submit&searchTerm=074137 Drugs@FDA]. U S Food and Drug Administration</ref>

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...artment of the Treasury]], and the Bureau of Drug Abuse Control, in the [[Food and Drug Administration]] in what was then the Department of Health, Education and Welfare (HEW). H

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...rchType=BasicSearch&Search_Button=Submit&searchTerm=076039 Drugs@FDA]. U S Food and Drug Administration</ref>

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Dificid brand of fidaxomicin was approved for Optimer Pharms by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve

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Levetiracetam was approved by the [[United States of America]] [[Food and Drug Administration]] ...r=Anonymous |authorlink= |coauthors= |date=1999 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=}}</ref>

...of Valid Genomic Biomarkers in the Context of Approved Drug Labels]. U.S. Food and Drug Administration</ref>.

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...or human-source research, such as the U.S. guidelines promulgated by the [[Food and Drug Administration]] (FDA).

Other participants in NACMCF include the [[Food and Drug Administration]] (FDA), the [[Centers for Disease Control]] (CDC), the [[National Marine F

...pplications/NewDrugApplicationNDA/default.htm New Drug Application] (NDA). Food and Drug Administration</ref> The NDA authorizes the drug to be advertised for specific '''indicat

Pepcid brand of famotidine was approved by the [[Food and Drug Administration]] in the [[United States of America]]. It is available as a generic, and al

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Inspra brand of eplerenone, submitted by GD Searle, was approved by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve

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...eatment. Reich was convicted, and died in prison (1957), for violating a [[Food and Drug Administration]] 1954 injunction against him for fraud in claims for what were called "org

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...U.S. proprietary name is '''Fortaz'''. Indications approved by the U.S. [[Food and Drug Administration]] include: infections with [[Pseudomonas aeruginosa]], [[Escherichia coli]]

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| [[Food and Drug Administration]] || 177 || [[Food and Drug Administration Police]]<ref name=prisonpolicyFleo04/>

...uthor=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-1 ...uthor=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-1

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As defined by the U.S. [[Food and Drug Administration]], each 100 milliliters contains:

...irus]]es. Four agents against influenza are currently approved by the US [[Food and Drug Administration]].

Auto-populated based on [[Special:WhatLinksHere/Food and Drug Administration]]. Needs checking by a human.

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Cellcept brand of mycophenolate mofetil was approved for Roche Palo by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve Mycophenolate mofetil is approved by the [[Food and Drug Administration]] in the [[United States of America]] for:

.../ref>, in which the precursors to the [[National Institutes of Health]], [[Food and Drug Administration]], the [[Social Security Administration]], and other well-known agencies, c

In the [[United States of America]], the [[Food and Drug Administration]] has approved the use of aripiprazole for the treatment of [[schizophrenia

...|authorlink= |coauthors= |date=09/20/2010 8 |format= |work= |publisher=US Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2011-02-2 ...authorlink= |coauthors= |date=August 1, 1991 |format= |work= |publisher=US Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-1

''Lexapro'' brand of escitalopram was approved by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve

Uses approved by the U.S. [[Food and Drug Administration]] are: ''[[Bacteroides]]'' brain sbscess, boutonneuse Fever, ''[[Hemophilus

'''Effexor''' brand of venlafaxine was approved by the [[Food and Drug Administration]] in the [[United States of America|United States]] with a [http://www.fda.

...been raised about possible side effects of the medication, prompting the [[Food and Drug Administration|FDA]] to add a Boxed Warning for Chantix’s label listing depressed mood,

Zetia brand of ezetimibe was approved for Merck and Schering-Plough by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve

The U.S. Food and Drug Administration (FDA) recognizes it as indicated for: [[glioma|glioblastoma multiforme]], m

...ntist]]. These medications are approved by national entities such as the [[Food and Drug Administration]] in the United States or by international entities such as the [[European United States [[Food and Drug Administration]] approved labels

...rchType=BasicSearch&Search_Button=Submit&searchTerm=075350 Drugs@FDA]. U S Food and Drug Administration</ref>

...nd superficial basal cell carcinoma; these indications are approved by the Food and Drug Administration. Other applications include actinic gheilitis, carcinoma in situ of the gla

...uses whose mothers had taken it during pregnancy. In response, the U.S. [[Food and Drug Administration]] banned its use in pregnancy.

...ively old drug, it is best known in the treatment of [[lymphoma]]s. U.S. [[Food and Drug Administration]] approved indications include: [[B-cell lymphoma]], [[Hodgkin's lymphoma]]

[[Celecoxib]] remains marketed and according to the [[Food and Drug Administration]] is indicated for the treatment of acute pain, various types of arthritis,

...fatness to the point of health impairment is enough of a concern that "the Food and Drug Administration yesterday cleared Pfizer Inc. to market a drug called Slentrol for use in t

...s |authorlink= |coauthors= |date=November, 2003 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-02-0 ...authorlink= |coauthors= |date=August 1, 1991 |format= |work= |publisher=US Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-1

...uivalence Code for [[generic drug]]s by the [[United States of America]] [[Food and Drug Administration]]. The table is from: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/F

*{{cite book| author=Food and Drug Administration (USA), Dockets Management Branch, Rockville, Maryland. Docket #82P-0316|tit

The underlying problem is easy to identify: who gets to decide? The U. S. [[Food and Drug Administration]] is supposed to prevent companies or individuals from marketing drugs or f

'''Labeled as approved uses''' by the U.S. [[Food and Drug Administration]]:<ref>{{citation

...r=Anonymous |authorlink= |coauthors= |date=2004 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-05-0

...g for patients with impaired renal function.<ref name="fda-renalcategories>Food and Drug Administration, Guidance for Industry: [http://www.fda.gov/Drugs/DevelopmentApprovalProces

...r=Anonymous |authorlink= |coauthors= |date=2008 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2008-11-0

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...e National Institute of Biomedical Imaging and Bioengineering (NIBIB), the Food and Drug Administration (FDA), private pharmaceutical companies and non-profit organizations, as a

*[http://www.fda.gov/ Food and Drug Administration] (FDA)

Cangrelor has not been approved for use in the United States by the [[Food and Drug Administration]]

Rivaroxaban was approved by the [[Food and Drug Administration]] in the [[United States of America]] 7/2011.<ref>Anonymous (2011) [http://

...United States]] it was not approved for the treatment of insomnia by the [[Food and Drug Administration]] until 1981 when it came out under the brand name ''Restoril''. It quickly