FdaApplication

ANDA 090329

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES INC
application_typeANDA
approval_date2014-07-03

Products (3)

ProductActive ingredientStrengthDosage form
CLONIDINE HYDROCHLORIDECLONIDINE HYDROCHLORIDE0.2MGTABLET;ORAL
CLONIDINE HYDROCHLORIDECLONIDINE HYDROCHLORIDE0.1MGTABLET;ORAL
CLONIDINE HYDROCHLORIDECLONIDINE HYDROCHLORIDE0.3MGTABLET;ORAL

3 products