FDAJuly 28, 2017drug

Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Tablet/Capsule Specification: out of specification for tablet weight.

What to do

FDA enforcement status: Terminated

Brands named

pd rx pharmaceuticals

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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