PlainRecalls
FDA Drug Moderate Class II Terminated

Alprazolam Extended-release Tablets, USP, 1 mg, 60-count bottle, Rx Only, Manufactured and Distributed by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-5022-91

Reported: May 31, 2017 Initiated: June 22, 2016 #D-0706-2017

Product Description

Alprazolam Extended-release Tablets, USP, 1 mg, 60-count bottle, Rx Only, Manufactured and Distributed by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-5022-91

Reason for Recall

Failed Dissolution Specifications

Details

Units Affected
24,176 bottles (1,450,560 tablets)
Distribution
Nationwide
Location
Morgantown, WV

Frequently Asked Questions

What product was recalled?
Alprazolam Extended-release Tablets, USP, 1 mg, 60-count bottle, Rx Only, Manufactured and Distributed by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-5022-91. Recalled by Mylan Pharmaceuticals Inc.. Units affected: 24,176 bottles (1,450,560 tablets).
Why was this product recalled?
Failed Dissolution Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on May 31, 2017. Severity: Moderate. Recall number: D-0706-2017.