PD-Rx Pharmaceuticals, Inc. recalls Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC
Recalled August 9, 2017 · FDA recall D-1057-2017 · PD-Rx Pharmaceuticals
Hazard
Failed Tablet/Capsule Specification: out of specification for tablet weight. · FDA Class II
Units
100 bottles
Sold at
Nationwide
Description
Failed Tablet/Capsule Specification: out of specification for tablet weight.
Product
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
Manufacturer(s)
PD-Rx Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →