PlainRecalls
FDA Drug Moderate Class II Terminated

Loxapine Capsules, USP 50 mg, Rx Only, 100-count bottles, NDC 0378-7050-01

Reported: May 30, 2018 Initiated: April 24, 2018 #D-0825-2018

Product Description

Loxapine Capsules, USP 50 mg, Rx Only, 100-count bottles, NDC 0378-7050-01

Reason for Recall

CGMP Deviations

Details

Units Affected
11,650 bottles
Distribution
Product was distributed throughout the United States, including Puerto Rico.
Location
Morgantown, WV

Frequently Asked Questions

What product was recalled?
Loxapine Capsules, USP 50 mg, Rx Only, 100-count bottles, NDC 0378-7050-01. Recalled by Mylan Pharmaceuticals Inc.. Units affected: 11,650 bottles.
Why was this product recalled?
CGMP Deviations
Which agency issued this recall?
This recall was issued by the FDA Drug on May 30, 2018. Severity: Moderate. Recall number: D-0825-2018.