FdaApplication

NDA 216185

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Identifiers

Properties

PropertyValue
applicant_nameAUCTA PHARMACEUTICALS INC
application_typeNDA
approval_date2023-05-04

Products (3)

ProductActive ingredientStrengthDosage form
MOTPOLY XRLACOSAMIDE150MGCAPSULE, EXTENDED RELEASE;ORAL
MOTPOLY XRLACOSAMIDE200MGCAPSULE, EXTENDED RELEASE;ORAL
MOTPOLY XRLACOSAMIDE100MGCAPSULE, EXTENDED RELEASE;ORAL

3 products