PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets NDC 55289-673-24; b) 30 tablets NDC 55289-673-30; c) 50 tablets NDC 55289-673-50; d) 60 tablets NDC 55289-673-60
Reported: February 7, 2018 Initiated: January 25, 2018 #D-0341-2018
Product Description
PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets NDC 55289-673-24; b) 30 tablets NDC 55289-673-30; c) 50 tablets NDC 55289-673-50; d) 60 tablets NDC 55289-673-60
Reason for Recall
CGMP deviations.
Details
- Recalling Firm
- PD-Rx Pharmaceuticals, Inc.
- Units Affected
- 7174 bottles
- Distribution
- Nationwide
- Location
- Oklahoma City, OK
Frequently Asked Questions
What product was recalled? ▼
PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets NDC 55289-673-24; b) 30 tablets NDC 55289-673-30; c) 50 tablets NDC 55289-673-50; d) 60 tablets NDC 55289-673-60. Recalled by PD-Rx Pharmaceuticals, Inc.. Units affected: 7174 bottles.
Why was this product recalled? ▼
CGMP deviations.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 7, 2018. Severity: Moderate. Recall number: D-0341-2018.
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