FdaApplication

NDA 018768

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Identifiers

Properties

PropertyValue
applicant_nameCORDEN PHARMA LATINA SPA
application_typeNDA
approval_date1983-11-10

Products (1)

ProductActive ingredientStrengthDosage form
VEPESIDETOPOSIDE20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INJECTION

1 product