Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
Reported: August 9, 2017 Initiated: July 28, 2017 #D-1057-2017
Product Description
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
Reason for Recall
Failed Tablet/Capsule Specification: out of specification for tablet weight.
Details
- Recalling Firm
- PD-Rx Pharmaceuticals, Inc.
- Units Affected
- 100 bottles
- Distribution
- Nationwide
- Location
- Oklahoma City, OK
Frequently Asked Questions
What product was recalled? ▼
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30. Recalled by PD-Rx Pharmaceuticals, Inc.. Units affected: 100 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsule Specification: out of specification for tablet weight.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 9, 2017. Severity: Moderate. Recall number: D-1057-2017.
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