FdaApplication

NDA 019183

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Identifiers

Properties

PropertyValue
applicant_nameABBVIE INC
application_typeNDA
approval_date1993-12-16

Products (1)

ProductActive ingredientStrengthDosage form
CARAFATESUCRALFATE1GM/10ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SUSPENSION;ORAL

1 product