FdaApplication

NDA 020406

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Identifiers

Properties

PropertyValue
applicant_nameTAKEDA PHARMACEUTICALS USA INC
application_typeNDA
approval_date1995-05-10

Products (2)

ProductActive ingredientStrengthDosage form
PREVACIDLANSOPRAZOLE15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, DELAYED REL PELLETS;ORAL
PREVACIDLANSOPRAZOLE30MGCAPSULE, DELAYED REL PELLETS;ORAL

2 products