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To view or add a comment, sign in FDA Duloxetine Recall: The FDA has announced a Class II recall of certain Duloxetine Delayed-Release Capsules after testing detected elevated levels of N-nitroso-duloxetine, a nitrosamine impurity that exceeds the FDA's recommended limits
Similar content being viewed by others Subjects Introduction The FDA estimates that acetaminophen (APAP) is the most widely used drug in the United States, with approximately 28 billion doses purchased per year 1
