FdaApplication

NDA 021689

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Identifiers

Properties

PropertyValue
applicant_nameASTRAZENECA PHARMACEUTICALS LP
application_typeNDA
approval_date2005-03-31

Products (2)

ProductActive ingredientStrengthDosage form
NEXIUM IVESOMEPRAZOLE SODIUMEQ 20MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INTRAVENOUS
NEXIUM IVESOMEPRAZOLE SODIUMEQ 40MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INTRAVENOUS

2 products