FdaApplication

ANDA 216592

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Identifiers

Properties

PropertyValue
applicant_nameGRANULES PHARMACEUTICALS INC
application_typeANDA
approval_date2023-07-13

Products (1)

ProductActive ingredientStrengthDosage form
ACETAMINOPHEN AND IBUPROFENACETAMINOPHEN; IBUPROFEN250MG;125MGTABLET;ORAL

1 product