Ohm Laboratories, Inc. recalls Ohm Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets, Distributed by Ohm Laboratories, Inc. 1385 L
Recalled October 21, 2015 · FDA recall D-0032-2016 · Ohm Laboratories
Hazard
Superpotent Drug: Out Of Specification (OOS) result for Assay. · FDA Class III
Units
311 boxes
Sold at
Nationwide.
Description
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Product
Ohm Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets, Distributed by Ohm Laboratories, Inc. 1385 Livingston Avenue, North Brunswick, NJ 08902, NDC 51660-527-31, UPC 3 5166052731 5
Manufacturer(s)
Ohm Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →