FdaApplication

ANDA 078885

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2009-03-09

Products (1)

ProductActive ingredientStrengthDosage form
LEUPROLIDE ACETATELEUPROLIDE ACETATE14MG/2.8ML (1MG/0.2ML)SOLUTION;SUBCUTANEOUS

1 product