FdaApplication

NDA 022056

Back to search

Identifiers

Properties

PropertyValue
applicant_nameAZURITY PHARMACEUTICALS INC
application_typeNDA
approval_date2008-03-20

Products (2)

ProductActive ingredientStrengthDosage form
PRILOSECOMEPRAZOLE MAGNESIUMEQ 2.5MG BASE/PACKETFOR SUSPENSION, DELAYED RELEASE;ORAL
PRILOSECOMEPRAZOLE MAGNESIUMEQ 10MG BASE/PACKETFOR SUSPENSION, DELAYED RELEASE;ORAL

2 products