PlainRecalls
FDA Drug Moderate Class II Terminated

Amlodipine Besylate Tablets, 10 mg Tablets, Packaged as A) 90 Count Bottles (NDC: 64679-423-01) and B) 1000 Count Bottles (NDC: 64679-423-02, Rx Only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA.

Reported: July 29, 2015 Initiated: April 22, 2015 #D-1256-2015

Product Description

Amlodipine Besylate Tablets, 10 mg Tablets, Packaged as A) 90 Count Bottles (NDC: 64679-423-01) and B) 1000 Count Bottles (NDC: 64679-423-02, Rx Only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA.

Reason for Recall

CGMP Deviations: Firm did not adequately investigate customer complaints.

Details

Recalling Firm
Wockhardt Usa Inc.
Units Affected
A) 152,164 Bottles and B) 50,991 Bottles.
Distribution
U.S. Nationwide including Puerto Rico.
Location
Parsippany, NJ

Frequently Asked Questions

What product was recalled?
Amlodipine Besylate Tablets, 10 mg Tablets, Packaged as A) 90 Count Bottles (NDC: 64679-423-01) and B) 1000 Count Bottles (NDC: 64679-423-02, Rx Only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA.. Recalled by Wockhardt Usa Inc.. Units affected: A) 152,164 Bottles and B) 50,991 Bottles..
Why was this product recalled?
CGMP Deviations: Firm did not adequately investigate customer complaints.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 29, 2015. Severity: Moderate. Recall number: D-1256-2015.