PlainRecalls
FDA Drug Low Class III Terminated

Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/80 mg, 30 Count Bottles, Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India. NDC: 43598-313-30.

Reported: September 2, 2015 Initiated: August 13, 2015 #D-1379-2015

Product Description

Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/80 mg, 30 Count Bottles, Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India. NDC: 43598-313-30.

Reason for Recall

Subpotent Drug: Subpotent atorvastatin.

Details

Units Affected
3840 Bottles
Distribution
U.S. Nationwide
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/80 mg, 30 Count Bottles, Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India. NDC: 43598-313-30.. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 3840 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-1379-2015.