FdaApplication

NDA 021799

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES INC
application_typeNDA
approval_date2005-08-12

Products (1)

ProductActive ingredientStrengthDosage form
QUALAQUINQUININE SULFATE324MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL

1 product