SUN PHARMACEUTICAL INDUSTRIES INC recalls Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10mg/240mg)
Recalled November 3, 2021 · FDA recall D-0068-2022 · SUN PHARMACEUTICAL INDUSTRIES
Hazard
Failed Moisture Limits · FDA Class III
Units
22,752 blister packs
Sold at
Nationwide within the United States
Description
Failed Moisture Limits
Product
Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10mg/240mg) , 10-count blister packs, Distributed By Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-5833-15
Manufacturer(s)
SUN PHARMACEUTICAL INDUSTRIES INC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →