PlainRecalls
FDA Drug Moderate Class II Terminated

Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 07207 USA, NDC 0228-2031-50

Reported: March 19, 2014 Initiated: February 10, 2014 #D-1153-2014

Product Description

Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 07207 USA, NDC 0228-2031-50

Reason for Recall

Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg.

Details

Recalling Firm
Actavis Elizabeth LLC
Units Affected
9447 Bottles
Distribution
Nationwide
Location
Elizabeth, NJ

Frequently Asked Questions

What product was recalled?
Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 07207 USA, NDC 0228-2031-50. Recalled by Actavis Elizabeth LLC. Units affected: 9447 Bottles.
Why was this product recalled?
Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 19, 2014. Severity: Moderate. Recall number: D-1153-2014.