FdaApplication

ANDA 071515

Back to search

Identifiers

Properties

PropertyValue
applicant_nameSUPERPHARM CORP
application_typeANDA
approval_date1988-06-08

Products (1)

ProductActive ingredientStrengthDosage form
PROPRANOLOL HYDROCHLORIDEPROPRANOLOL HYDROCHLORIDE10MGTABLET;ORAL

1 product