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FDA ANDA · ANDA090150

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Sponsor: APOTEX

APPLICATION
ANDA090150
TYPE
ANDA
ORIGINAL APPROVAL
2010-08-11
LATEST ACTION
2017-02-24
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDEDiscontinued
HYDROCHLOROTHIAZIDE 25MG, LOSARTAN POTASSIUM 100MG · TABLET · ORAL
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDEDiscontinued
HYDROCHLOROTHIAZIDE 12.5MG, LOSARTAN POTASSIUM 50MG · TABLET · ORAL
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDEDiscontinued
HYDROCHLOROTHIAZIDE 12.5MG, LOSARTAN POTASSIUM 100MG · TABLET · ORAL

Approval history

2017-02-24Labeling · Supplement 10 · standardAP
2015-11-05Labeling · Supplement 4 · standardAP
2015-05-01Labeling · Supplement 8 · standardAP
2015-05-01Labeling · Supplement 6 · standardAP
2015-05-01Labeling · Supplement 9 · standardAP
2015-05-01Labeling · Supplement 7 · standardAP
2010-10-06OriginalAP
2010-08-11OriginalAP
VIEW ON DRUGS@FDA ↗

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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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