FdaApplication

ANDA 088828

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Identifiers

Properties

PropertyValue
applicant_nameSUPERPHARM CORP
application_typeANDA
approval_date1984-12-28

Products (1)

ProductActive ingredientStrengthDosage form
HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE50MGTABLET;ORAL

1 product