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FDA ANDA · ANDA078359

DESLORATADINE

Sponsor: SUN PHARM INDS

APPLICATION
ANDA078359
TYPE
ANDA
ORIGINAL APPROVAL
2010-11-16
LATEST ACTION
2019-10-22
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

DESLORATADINEDiscontinued
DESLORATADINE 5MG · TABLET · ORAL

Approval history

2019-10-22Labeling · Supplement 3 · standardAP
2019-10-22Labeling · Supplement 8 · standardAP
2013-10-07Labeling · Supplement 1 · standardAP
2010-11-16OriginalAP
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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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