FdaApplication

ANDA 090082

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2010-06-17

Products (4)

ProductActive ingredientStrengthDosage form
ALPRAZOLAMALPRAZOLAM1MGTABLET;ORAL
ALPRAZOLAMALPRAZOLAM0.25MGTABLET;ORAL
ALPRAZOLAMALPRAZOLAM0.5MGTABLET;ORAL
ALPRAZOLAMALPRAZOLAM2MGTABLET;ORAL

4 products