FdaApplication

NDA 019649

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES INC
application_typeNDA
approval_date1993-09-17

Products (1)

ProductActive ingredientStrengthDosage form
FLUMADINERIMANTADINE HYDROCHLORIDE100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET;ORAL

1 product