FdaApplication

ANDA 218385

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Identifiers

Properties

PropertyValue
applicant_nameGRANULES PHARMACEUTICALS INC
application_typeANDA
approval_date2024-10-17

Products (3)

ProductActive ingredientStrengthDosage form
BUPROPION HYDROCHLORIDEBUPROPION HYDROCHLORIDE200MGTABLET, EXTENDED RELEASE;ORAL
BUPROPION HYDROCHLORIDEBUPROPION HYDROCHLORIDE100MGTABLET, EXTENDED RELEASE;ORAL
BUPROPION HYDROCHLORIDEBUPROPION HYDROCHLORIDE150MGTABLET, EXTENDED RELEASE;ORAL

3 products