FdaApplication

ANDA 065356

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2006-05-31

Products (4)

ProductActive ingredientStrengthDosage form
DOXYCYCLINEDOXYCYCLINEEQ 50MG BASETABLET;ORAL
DOXYCYCLINEDOXYCYCLINEEQ 75MG BASETABLET;ORAL
DOXYCYCLINEDOXYCYCLINEEQ 100MG BASETABLET;ORAL
DOXYCYCLINEDOXYCYCLINEEQ 150MG BASETABLET;ORAL

4 products