FdaApplication

ANDA 070459

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Identifiers

Properties

PropertyValue
applicant_namePAR PHARMACEUTICAL INC
application_typeANDA
approval_date1986-07-08

Products (1)

ProductActive ingredientStrengthDosage form
CLONIDINE HYDROCHLORIDECLONIDINE HYDROCHLORIDE0.3MGTABLET;ORAL

1 product