FdaApplication

NDA 019599

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Identifiers

Properties

PropertyValue
applicant_nameLEGACY PHARMA INC SEZC
application_typeNDA
approval_date1988-02-29

Products (2)

ProductActive ingredientStrengthDosage form
NAFTINNAFTIFINE HYDROCHLORIDE1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CREAM;TOPICAL
NAFTINNAFTIFINE HYDROCHLORIDE2%CREAM;TOPICAL

2 products