FdaApplication

ANDA 078619

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Identifiers

Properties

PropertyValue
applicant_nameAUROBINDO PHARMA LTD
application_typeANDA
approval_date2008-01-31

Products (3)

ProductActive ingredientStrengthDosage form
FLUOXETINE HYDROCHLORIDEFLUOXETINE HYDROCHLORIDEEQ 10MG BASECAPSULE;ORAL
FLUOXETINE HYDROCHLORIDEFLUOXETINE HYDROCHLORIDEEQ 20MG BASECAPSULE;ORAL
FLUOXETINE HYDROCHLORIDEFLUOXETINE HYDROCHLORIDEEQ 40MG BASECAPSULE;ORAL

3 products