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FDA ANDA · ANDA090385

LEVOCETIRIZINE DIHYDROCHLORIDE

Sponsor: GLENMARK PHARMS LTD

APPLICATION
ANDA090385
TYPE
ANDA
ORIGINAL APPROVAL
2011-02-24
LATEST ACTION
2025-07-11
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription

Products

LEVOCETIRIZINE DIHYDROCHLORIDEPrescription
LEVOCETIRIZINE DIHYDROCHLORIDE 5MG · TABLET · ORAL

Approval history

2025-07-11Labeling · Supplement 18 · standardAP
2020-11-05Labeling · Supplement 12 · standardAP
2018-06-27Labeling · Supplement 9 · standardAP
2018-06-27Labeling · Supplement 7 · standardAP
2018-06-27Labeling · Supplement 5 · standardAP
2018-06-27Labeling · Supplement 8 · standardAP
2018-06-27Labeling · Supplement 6 · standardAP
2015-11-25Labeling · Supplement 4 · standardAP
2013-11-29Labeling · Supplement 3 · standardAP
2013-02-05Labeling · Supplement 2 · standardAP
2011-02-24OriginalAP
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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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