FdaApplication

ANDA 075662

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Identifiers

Properties

PropertyValue
applicant_nameWATSON LABORATORIES INC
application_typeANDA
approval_date2002-01-29

Products (2)

ProductActive ingredientStrengthDosage form
FLUOXETINEFLUOXETINE HYDROCHLORIDEEQ 10MG BASECAPSULE;ORAL
FLUOXETINEFLUOXETINE HYDROCHLORIDEEQ 20MG BASECAPSULE;ORAL

2 products