FdaApplication

NDA 019880

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Identifiers

Properties

PropertyValue
applicant_nameCORDEN PHARMA LATINA SPA
application_typeNDA
approval_date1989-03-03

Products (3)

ProductActive ingredientStrengthDosage form
PARAPLATINCARBOPLATIN50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INJECTION
PARAPLATINCARBOPLATIN150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INJECTION
PARAPLATINCARBOPLATIN450MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INJECTION

3 products