FdaApplication

NDA 018285

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Identifiers

Properties

PropertyValue
applicant_nameNOVARTIS PHARMACEUTICALS CORP
application_typeNDA
approval_date1982-09-03

Products (2)

ProductActive ingredientStrengthDosage form
VISKENPINDOLOL10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET;ORAL
VISKENPINDOLOL5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET;ORAL

2 products