FdaApplication

ANDA 215568

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Identifiers

Properties

PropertyValue
applicant_nameGRANULES PHARMACEUTICALS INC
application_typeANDA
approval_date2022-02-02

Products (2)

ProductActive ingredientStrengthDosage form
BUPROPION HYDROCHLORIDEBUPROPION HYDROCHLORIDE300MGTABLET, EXTENDED RELEASE;ORAL
BUPROPION HYDROCHLORIDEBUPROPION HYDROCHLORIDE150MGTABLET, EXTENDED RELEASE;ORAL

2 products