FdaApplication

NDA 022525

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Identifiers

Properties

PropertyValue
applicant_nameABBVIE INC
application_typeNDA
approval_date2010-06-21

Products (4)

ProductActive ingredientStrengthDosage form
NAMENDA XRMEMANTINE HYDROCHLORIDE21MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE;ORAL
NAMENDA XRMEMANTINE HYDROCHLORIDE7MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE;ORAL
NAMENDA XRMEMANTINE HYDROCHLORIDE28MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE;ORAL
NAMENDA XRMEMANTINE HYDROCHLORIDE14MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE;ORAL

4 products