Valeant Pharmaceuticals North America LLC recalls Diltiazem HCl CD capsules, 360 mg, 90-count bottles, Rx Only, Manufactured for: Oceanside Pharmaceuticals, a division of
Recalled February 20, 2019 · FDA recall D-0491-2019 · Valeant Pharmaceuticals North America
Hazard
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points. · FDA Class III
Units
23,884 bottles
Sold at
Nationwide in the USA and Puerto Rico
Description
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Product
Diltiazem HCl CD capsules, 360 mg, 90-count bottles, Rx Only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7 Canada; NDC 68682-521-01.
Manufacturer(s)
Valeant Pharmaceuticals North America LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →