PlainRecalls
FDA Drug Moderate Class II Terminated

Alprazolam Tablets, USP, 0.25 mg, 100-count Unit Dose tablets per carton, Rx Only, Manufactured by: Watson Pharma Private Limited, Verna, Salcette Goa 403 722 INDIA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-5858-61.

Reported: October 25, 2017 Initiated: September 26, 2017 #D-0013-2018

Product Description

Alprazolam Tablets, USP, 0.25 mg, 100-count Unit Dose tablets per carton, Rx Only, Manufactured by: Watson Pharma Private Limited, Verna, Salcette Goa 403 722 INDIA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-5858-61.

Reason for Recall

Failed Impurities/Degradation Specifications: Out-of-specification result for an unknown impurity.

Details

Recalling Firm
The Harvard Drug Group
Units Affected
3,935 cartons
Distribution
Nationwide in the USA
Location
Livonia, MI

Frequently Asked Questions

What product was recalled?
Alprazolam Tablets, USP, 0.25 mg, 100-count Unit Dose tablets per carton, Rx Only, Manufactured by: Watson Pharma Private Limited, Verna, Salcette Goa 403 722 INDIA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-5858-61.. Recalled by The Harvard Drug Group. Units affected: 3,935 cartons.
Why was this product recalled?
Failed Impurities/Degradation Specifications: Out-of-specification result for an unknown impurity.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 25, 2017. Severity: Moderate. Recall number: D-0013-2018.