FdaApplication

ANDA 076911

Back to search

Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2004-09-29

Products (3)

ProductActive ingredientStrengthDosage form
CLORAZEPATE DIPOTASSIUMCLORAZEPATE DIPOTASSIUM15MGTABLET;ORAL
CLORAZEPATE DIPOTASSIUMCLORAZEPATE DIPOTASSIUM3.75MGTABLET;ORAL
CLORAZEPATE DIPOTASSIUMCLORAZEPATE DIPOTASSIUM7.5MGTABLET;ORAL

3 products