FdaApplication

ANDA 071516

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Identifiers

Properties

PropertyValue
applicant_nameSUPERPHARM CORP
application_typeANDA
approval_date1988-06-08

Products (1)

ProductActive ingredientStrengthDosage form
PROPRANOLOL HYDROCHLORIDEPROPRANOLOL HYDROCHLORIDE20MGTABLET;ORAL

1 product