FdaApplication

ANDA 065053

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2000-11-22

Products (3)

ProductActive ingredientStrengthDosage form
DOXYCYCLINEDOXYCYCLINEEQ 50MG BASECAPSULE;ORAL
DOXYCYCLINEDOXYCYCLINEEQ 100MG BASECAPSULE;ORAL
DOXYCYCLINEDOXYCYCLINEEQ 75MG BASECAPSULE;ORAL

3 products