FdaApplication

NDA 020886

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Identifiers

Properties

PropertyValue
applicant_nameADVANZ PHARMA (US) CORP
application_typeNDA
approval_date1999-02-02

Products (1)

ProductActive ingredientStrengthDosage form
PANRETINALITRETINOINEQ 0.1% BASEGEL;TOPICAL

1 product