FdaApplication

NDA 020949

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Identifiers

Properties

PropertyValue
applicant_namePHARMOBEDIENT CONSULTING LLC
application_typeNDA
approval_date2001-04-30

Products (2)

ProductActive ingredientStrengthDosage form
ACCUNEBALBUTEROL SULFATEEQ 0.021% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SOLUTION;INHALATION
ACCUNEBALBUTEROL SULFATEEQ 0.042% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SOLUTION;INHALATION

2 products