FdaApplication

NDA 022511

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Identifiers

Properties

PropertyValue
applicant_nameHORIZON MEDICINES LLC
application_typeNDA
approval_date2010-04-30

Products (2)

ProductActive ingredientStrengthDosage form
VIMOVOESOMEPRAZOLE MAGNESIUM; NAPROXENEQ 20MG BASE;375MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, DELAYED RELEASE;ORAL
VIMOVOESOMEPRAZOLE MAGNESIUM; NAPROXENEQ 20MG BASE;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET, DELAYED RELEASE;ORAL

2 products