FdaApplication

ANDA 040810

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES INC
application_typeANDA
approval_date2007-03-27

Products (2)

ProductActive ingredientStrengthDosage form
HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE50MGTABLET;ORAL
HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE25MGTABLET;ORAL

2 products