FdaApplication

ANDA 076041

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2002-12-24

Products (3)

ProductActive ingredientStrengthDosage form
SOTRETISOTRETINOIN10MGCAPSULE;ORAL
SOTRETISOTRETINOIN40MGCAPSULE;ORAL
SOTRETISOTRETINOIN20MGCAPSULE;ORAL

3 products