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FDA ANDA · ANDA091567

FEXOFENADINE HYDROCHLORIDE

Sponsor: SUN PHARM INDS

APPLICATION
ANDA091567
TYPE
ANDA
ORIGINAL APPROVAL
2012-02-06
LATEST ACTION
2015-02-25
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Over-the-counter, Discontinued

Products

FEXOFENADINE HYDROCHLORIDE ALLERGYOver-the-counter
FEXOFENADINE HYDROCHLORIDE 180MG · TABLET · ORAL
FEXOFENADINE HYDROCHLORIDE ALLERGYDiscontinued
FEXOFENADINE HYDROCHLORIDE 60MG · TABLET · ORAL
CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGYDiscontinued
FEXOFENADINE HYDROCHLORIDE 30MG · TABLET · ORAL
FEXOFENADINE HYDROCHLORIDE HIVESOver-the-counter
FEXOFENADINE HYDROCHLORIDE 180MG · TABLET · ORAL
FEXOFENADINE HYDROCHLORIDE HIVESDiscontinued
FEXOFENADINE HYDROCHLORIDE 60MG · TABLET · ORAL
CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVESDiscontinued
FEXOFENADINE HYDROCHLORIDE 30MG · TABLET · ORAL

Approval history

2015-02-25Manufacturing (CMC) · Supplement 1 · unknownAP
2012-02-06OriginalAP
VIEW ON DRUGS@FDA ↗

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