FdaApplication

ANDA 090931

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2010-07-15

Products (1)

ProductActive ingredientStrengthDosage form
TAMSULOSIN HYDROCHLORIDETAMSULOSIN HYDROCHLORIDE0.4MGCAPSULE;ORAL

1 product