FdaApplication

ANDA 088570

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES INC
application_typeANDA
approval_date1984-04-10

Products (1)

ProductActive ingredientStrengthDosage form
RESERPINE, HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEHYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE25MG;15MG;0.1MGTABLET;ORAL

1 product