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
- Recalling Firm
- PD-Rx Pharmaceuticals, Inc.
- 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.
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