VIVITROL (naltrexone for extended-release injectable suspension); 380 mg vial NDC 65757-300-01; RX Only Manufactured and marketed by Alkermes, Inc., Waltham, MA 02451.
Recall Number: D-1556-2014
Firm: Alkermes, Inc.
Classification: Class II
Status: Terminated
Report Date: 20140903
Initiation Date: 20140304
Termination Date: 20141222
Reason for Recall
Customer complaints for failure to deliver the dose.
Product Description
VIVITROL (naltrexone for extended-release injectable suspension); 380 mg vial NDC 65757-300-01; RX Only Manufactured and marketed by Alkermes, Inc., Waltham, MA 02451.