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FDA NDA · NDA021721

LEVAQUIN

Sponsor: JANSSEN PHARMS

APPLICATION
NDA021721
TYPE
NDA
ORIGINAL APPROVAL
2004-10-21
LATEST ACTION
2017-02-08
ROUTE
ORAL
DOSAGE FORM
SOLUTION
MARKETING STATUS
Discontinued

Products

LEVAQUIN · ReferenceDiscontinued
LEVOFLOXACIN 250MG/10ML · SOLUTION · ORAL

Approval history

2017-02-08Labeling · Supplement 35 · standardLetterAP
2016-07-26Labeling · Supplement 34 · standardLabelAP
2014-05-23Labeling · Supplement 33 · standardLabelAP
2013-08-14Labeling · Supplement 32 · 901 requiredLetterAP
2012-04-27Efficacy · Supplement 28 · priorityLabelAP
2011-10-11Labeling · Supplement 29 · unknownLabelAP
2011-10-11REMS · Supplement 31ReviewAP
2011-06-09Labeling · Supplement 26 · standardLabelAP
2011-02-25Labeling · Supplement 25 · 901 requiredLabelAP
2009-04-27Labeling · Supplement 21 · standardLetterAP
2009-03-12Labeling · Supplement 22 · standardLetterAP
2008-10-03Labeling · Supplement 20 · standardLetterAP
2008-05-05Efficacy · Supplement 15 · unknownSummary ReviewAP
2008-04-16Labeling · Supplement 19 · standardLabelAP
2007-12-13Labeling · Supplement 18 · standardLetterAP
2007-11-16Labeling · Supplement 17 · standardLetterAP
2007-11-15Labeling · Supplement 16 · standardLabelAP
2007-09-14Efficacy · Supplement 9 · unknownLabelAP
2007-09-11Efficacy · Supplement 11 · priorityLabelAP
2007-06-19Labeling · Supplement 13 · standardLabelAP
2007-05-31Labeling · Supplement 10 · standardLetterAP
2007-05-10Labeling · Supplement 12 · standardLetterAP
2006-06-23Labeling · Supplement 7 · standardLetterAP
2006-01-20Labeling · Supplement 6 · standardLabelAP
2005-08-04Efficacy · Supplement 2 · unknownLabelAP
2004-11-24Efficacy · Supplement 3 · priorityLabelAP
2004-10-21Type 3 - New Dosage Form · Original · standardMedication GuideAP
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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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