Dr. Reddy's Laboratories, Inc. recalls Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-318-30) a
Recalled September 2, 2015 · FDA recall D-1377-2015 · Dr. Reddy's Laboratories
Hazard
Subpotent Drug: Subpotent atorvastatin. · FDA Class III
Units
a) 16,080 and b) 480 Bottles
Sold at
U.S. Nationwide
Description
Subpotent Drug: Subpotent atorvastatin.
Product
Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-318-30) and b) 90 Count Bottles (NDC: 43598-318-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →