FdaApplication

ANDA 077926

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2008-09-19

Products (3)

ProductActive ingredientStrengthDosage form
CARBOPLATINCARBOPLATIN50MG/5ML (10MG/ML)INJECTABLE;INTRAVENOUS
CARBOPLATINCARBOPLATIN450MG/45ML (10MG/ML)INJECTABLE;INTRAVENOUS
CARBOPLATINCARBOPLATIN150MG/15ML (10MG/ML)INJECTABLE;INTRAVENOUS

3 products