FdaApplication

ANDA 077569

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Identifiers

Properties

PropertyValue
applicant_nameLANDELA PHARMACEUTICAL
application_typeANDA
approval_date2006-04-04

Products (1)

ProductActive ingredientStrengthDosage form
ALBUTEROL SULFATEALBUTEROL SULFATEEQ 0.083% BASESOLUTION;INHALATION

1 product