Duragesic Pain Patch Recall News

April 7, 2004
KEY INFORMATION FOR PATIENTS AND CAREGIVERS
Janssen Pharmaceutica Products, L.P. announced an expanded recall to users of DURAGESIC (fentanyl transdermal system) CII 75 mcg/hour, NDC #50458-035-05, control numbers 0327192 (exp. 10/05), 0327193 (exp. 10/05), 0327294 (exp. 11/05), 0327295 (exp. 11/05) and 0330362 (exp. 12/05)
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July 15, 2005
U.S. Warns Fentanyl Patients About Drug
The government is investigating 120 deaths among users of patches that emit the painkiller fentanyl and warned patients Friday to be sure to use the powerful narcotic properly to avoid accidental overdose.
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Click here to visit the FDA's page on Fentanyl Transdermal System (marketed as Duragesic) Information

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