FdaApplication

ANDA 075526

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES INC
application_typeANDA
approval_date2002-09-26

Products (1)

ProductActive ingredientStrengthDosage form
TICLOPIDINE HYDROCHLORIDETICLOPIDINE HYDROCHLORIDE250MGTABLET;ORAL

1 product