FdaApplication

NDA 208647

Back to search

Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeNDA
approval_date2018-12-18

Products (4)

ProductActive ingredientStrengthDosage form
EZALLOR SPRINKLEROSUVASTATIN CALCIUMEQ 5MG BASECAPSULE;ORAL
EZALLOR SPRINKLEROSUVASTATIN CALCIUMEQ 40MG BASECAPSULE;ORAL
EZALLOR SPRINKLEROSUVASTATIN CALCIUMEQ 10MG BASECAPSULE;ORAL
EZALLOR SPRINKLEROSUVASTATIN CALCIUMEQ 20MG BASECAPSULE;ORAL

4 products