Class II
Terminated
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
- Company
- Pd-Rx Pharmaceuticals, Inc.
- Recall Initiated
- July 28, 2017
- Posted
- August 9, 2017
- Recall Number
- D-1057-2017
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 100 bottles
- Firm Location
- Oklahoma City, OK, United States
Reason for Recall
Failed Tablet/Capsule Specification: out of specification for tablet weight.
Distribution
Nationwide
Lot / Code Info
Lot: A17F55 Exp. 06/30/2018
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