FdaApplication

ANDA 075588

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Identifiers

Properties

PropertyValue
applicant_nameCONTRACT PHARMACAL CORP
application_typeANDA
approval_date2002-04-08

Products (1)

ProductActive ingredientStrengthDosage form
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDEIBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE200MG;30MGTABLET;ORAL

1 product