PlainRecalls
FDA Drug Moderate Class II Terminated

Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottles, Rx only, Packaged by PD-RX Pharmaceuticals, Inc., Oklahoma City, OK 73127, MFG: Mutual Pharm. Co. Inc., Philadelphia, PA 19124, NDC 43063-509-01

Reported: January 6, 2016 Initiated: July 10, 2015 #D-0559-2016

Product Description

Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottles, Rx only, Packaged by PD-RX Pharmaceuticals, Inc., Oklahoma City, OK 73127, MFG: Mutual Pharm. Co. Inc., Philadelphia, PA 19124, NDC 43063-509-01

Reason for Recall

cGMP Deviations

Details

Units Affected
9 bottles
Distribution
Alabama
Location
Oklahoma City, OK

Frequently Asked Questions

What product was recalled?
Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottles, Rx only, Packaged by PD-RX Pharmaceuticals, Inc., Oklahoma City, OK 73127, MFG: Mutual Pharm. Co. Inc., Philadelphia, PA 19124, NDC 43063-509-01. Recalled by PD-Rx Pharmaceuticals, Inc.. Units affected: 9 bottles.
Why was this product recalled?
cGMP Deviations
Which agency issued this recall?
This recall was issued by the FDA Drug on January 6, 2016. Severity: Moderate. Recall number: D-0559-2016.