KVK-Tech, Inc. recalls Hydrocodone Bitartrate and Homatropine Methlybromide tablets, USP, 5 mg/ 1.5 mg, 30-count bottle, Rx only, Mfd. By:KVK-T
Recalled May 26, 2021 · FDA recall D-0386-2021 · KVK-Tech
Hazard
Failed Impurities/Degradation Specifications · FDA Class III
Units
17,096 bottles
Sold at
Distributed Nationwide in the USA
Description
Failed Impurities/Degradation Specifications
Product
Hydrocodone Bitartrate and Homatropine Methlybromide tablets, USP, 5 mg/ 1.5 mg, 30-count bottle, Rx only, Mfd. By:KVK-Tech, Inc., Newtown, PA, 18940 NDC 10702-055-03
Manufacturer(s)
KVK-Tech, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →