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- ...ssion]], which ultimately leads to cell [[lysis]]. Ampicillin has received FDA approval for its action of mechanism.7 KB (881 words) - 16:47, 27 September 2010
- ...Administration. [http://www.fda.gov/bbs/topics/ANSWERS/2004/ANS01329.html "FDA Strengthens Labels of Two Specific Types of Antibiotics to Ensure Proper Us4 KB (483 words) - 16:48, 27 September 2010
- ...http://www.merck.com/newsroom/news-release-archive/product/2009_1201a.html FDA Approves Zegerid OTC for Over-the-Counter Treatment of Frequent Heartburn]. ...1995. URL: [http://www.fda.gov/fdac/features/695_prescrip.html http://www.fda.gov/fdac/features/695_prescrip.html]. Accessed on: June 11, 2006.</ref> Un17 KB (2,299 words) - 09:15, 5 September 2010
- On April 25, 2008 the FDA issued a press release<ref>http://www.fda.gov/oc/po/firmrecalls/actavis04_08.html</ref> alerting the public to a Clas On March 31, 2009 the FDA announced another generic digoxin pill recall by posting this company press19 KB (2,738 words) - 16:48, 27 September 2010
- ...ks. The highest approved dose of simvastatin is 80 mg.<ref>http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders ...name="urlInformation on Simvastatin/Amiodarone">{{cite web |url=http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders14 KB (1,967 words) - 16:48, 27 September 2010
- ...lymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=11119 |title=FDA drug information, acetazolamide capsule, extended release | author= | publi12 KB (1,686 words) - 16:48, 27 September 2010
- Under FDA rules, this drug, like many others, excludes eligibility for blood donation11 KB (1,410 words) - 16:49, 27 September 2010
- ...d Drug Administration (United States)|U.S. Food and Drug Administration]] (FDA) in April 2005 mandated that all (including salbutamol) inhalers containing ...re patented. An industry consortium was formed to spread the costs of the FDA safety studies to get propellants such as 134a and 227 approved.<ref>[http:15 KB (2,005 words) - 16:49, 27 September 2010
- ...ww.fda.gov/newsevents/newsroom/pressannouncements/ucm149533.htm]</ref> The FDA only approves metoclopramide for 4-12 week short term treatment. ...=U.S. Food and Drug Administration |date=February 26, 2009 |url=http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm149533.htm |accessdate=2009-011 KB (1,453 words) - 16:49, 27 September 2010
- .../www.rxlist.com/cgi/generic/ibup.htm Motrin (Ibuprofen) drug description - FDA approved labeling for prescription drugs and medications at RxList<!-- Bot ...47.html |title=FDA Approves Caldolor: Cumberland Pharmaceuticals Announces FDA Approval of Caldolor |date=June 11, 2009 |publisher=Drugs.com |accessdate=229 KB (3,955 words) - 22:17, 21 September 2010
- ...e assembly of [[Boyle's machine]]s. Because India's Food & Drug Authority (FDA-India) rules state that transferring a drug from one container to another (61 KB (8,728 words) - 16:50, 27 September 2010
- ...hough this use is in decline.<ref>{{cite web|author = FDA|url = http://www.fda.gov/Cber/vaccine/thimerosal.htm|title = Thimerosal in Vaccines|accessdate=O ...tivated influenza vaccine.<ref>{{cite web |date=2007-09-06 |url=http://www.fda.gov/cber/vaccine/thimerosal.htm |accessdate=2007-10-01 |title= Thimerosal i69 KB (10,077 words) - 21:35, 20 September 2010
- ...uld later prove useful. Zidovudine (AZT) was approved for marketing by the FDA on March 20, 1987.<ref name="Cimons">{{cite news | last = Cimons | first = ...) approved the drug (via the then-new [[FDA Fast Track Development Program|FDA accelerated approval system]]) for use against HIV, AIDS, and ''AIDS Relate21 KB (3,049 words) - 16:51, 27 September 2010
- ...ower than 2.5 grams per day.<ref name="2009_FDA_support">"[http://www.fda.gov/downloads/AdvisoryCommittees/CommitteesMeetingMaterials/Drugs/DrugSafet ...[http://www.fda.gov/Drugs/DrugSafety/InformationbyDrugClass/ucm165107.htm "FDA: Drug Safety & Availability - Acetaminophen Information"]</ref>54 KB (7,376 words) - 16:52, 27 September 2010
- ...Circuit|U.S. Court of Appeals for the Tenth Circuit]] in Denver upheld the FDA's final rule declaring all dietary supplements containing ephedrine alkaloi21 KB (2,906 words) - 16:51, 27 September 2010
- ...as approved by the American [[Food and Drug Administration (United States)|FDA]] in January 2008. ...title=MiddleBrook Pharmaceuticals Launches MOXATAG(TM), the First and Only FDA-Approved Once-Daily Amoxicillin |year=2009 | month=March| url=http://www.mi11 KB (1,413 words) - 16:52, 27 September 2010
- | work = FDA Poisonous Plant Database | url = http://vm.cfsan.fda.gov/~djw/pltx.cgi?QUERY=tephrosia3 KB (345 words) - 12:27, 7 July 2010
- ...(United States)|U.S. Food and Drug Administration]] (FDA).<ref>[http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/EnforcementActi19 KB (2,832 words) - 12:27, 7 July 2010
- ...is no antidote. Despite its [[toxicity]], colchicine is approved by the US FDA for the treatment of [[gout]] and [[Familial Mediterranean Fever]] and is a4 KB (471 words) - 12:27, 7 July 2010
- ...ov/ohrms/dockets/dailys/03/jul03/070303/81N-0033P_emc-000001.txt Letter to FDA], Professor George T. Gallagher, [[Boston University]] [[Goldman School of | url = http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/EnforcementActivitiesbyFD14 KB (2,005 words) - 12:27, 7 July 2010