PlainRecalls
FDA Drug Low Class III Terminated

Amlodipine besylate and Atorvastatin calcium Tablets, 5 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-319-30) and b) 90 Count Bottles (NDC: 43598-319-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India.

Reported: September 2, 2015 Initiated: August 13, 2015 #D-1376-2015

Product Description

Amlodipine besylate and Atorvastatin calcium Tablets, 5 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-319-30) and b) 90 Count Bottles (NDC: 43598-319-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India.

Reason for Recall

Subpotent Drug: Subpotent atorvastatin.

Details

Units Affected
a) 14,640 and b) 624 Bottles
Distribution
U.S. Nationwide
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
Amlodipine besylate and Atorvastatin calcium Tablets, 5 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-319-30) and b) 90 Count Bottles (NDC: 43598-319-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India.. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: a) 14,640 and b) 624 Bottles.
Why was this product recalled?
Subpotent Drug: Subpotent atorvastatin.
Which agency issued this recall?
This recall was issued by the FDA Drug on September 2, 2015. Severity: Low. Recall number: D-1376-2015.