FdaApplication

NDA 020819

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Identifiers

Properties

PropertyValue
applicant_nameABBVIE INC
application_typeNDA
approval_date1998-04-17

Products (3)

ProductActive ingredientStrengthDosage form
ZEMPLARPARICALCITOL0.01MG/2ML (0.005MG/ML)SOLUTION;INTRAVENOUS
ZEMPLARPARICALCITOL0.005MG/ML (0.005MG/ML)SOLUTION;INTRAVENOUS
ZEMPLARPARICALCITOL0.002MG/ML (0.002MG/ML)SOLUTION;INTRAVENOUS

3 products