FdaApplication

ANDA 088962

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Identifiers

Properties

PropertyValue
applicant_nameSUPERPHARM CORP
application_typeANDA
approval_date1985-05-10

Products (1)

ProductActive ingredientStrengthDosage form
LOGENATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE0.025MG;2.5MGTABLET;ORAL

1 product