FdaApplication

ANDA 071726

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Identifiers

Properties

PropertyValue
applicant_nameNEPHRON PHARMACEUTICALS CORP
application_typeANDA
approval_date1988-07-14

Products (1)

ProductActive ingredientStrengthDosage form
METAPROTERENOL SULFATEMETAPROTERENOL SULFATE0.6%SOLUTION;INHALATION

1 product