FdaApplication

NDA 021520

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Identifiers

Properties

PropertyValue
applicant_nameELI LILLY AND CO
application_typeNDA
approval_date2003-12-24

Products (5)

ProductActive ingredientStrengthDosage form
SYMBYAXFLUOXETINE HYDROCHLORIDE; OLANZAPINEEQ 50MG BASE;EQ 6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL
SYMBYAXFLUOXETINE HYDROCHLORIDE; OLANZAPINEEQ 25MG BASE;EQ 6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL
SYMBYAXFLUOXETINE HYDROCHLORIDE; OLANZAPINEEQ 25MG BASE;EQ 12MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL
SYMBYAXFLUOXETINE HYDROCHLORIDE; OLANZAPINEEQ 25MG BASE;EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL
SYMBYAXFLUOXETINE HYDROCHLORIDE; OLANZAPINEEQ 50MG BASE;EQ 12MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL

5 products