Sun Pharmaceutical Industries, Inc. recalls Carvediol Tablets , USP, 3.125 mg, 100-count bottle (NDC 57664-242-88). 500-count bottle (NDC 57664-242-13), 1000-count
Recalled September 28, 2016 · FDA recall D-1504-2016 · Sun Pharmaceutical Industries
Hazard
Failed Impurities/Degradation Specifications · FDA Class III
Units
4,656 HDPE bottles
Sold at
Nationwide
Description
Failed Impurities/Degradation Specifications
Product
Carvediol Tablets , USP, 3.125 mg, 100-count bottle (NDC 57664-242-88). 500-count bottle (NDC 57664-242-13), 1000-count bottle (NDC 57664-242-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512
Manufacturer(s)
Sun Pharmaceutical Industries, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →