Sulfamethoxazole and Trimethoprim Tablets, 800 mg/160 mg, DOUBLE STRENGTH, Rx, packaged and labeled to contain Sulfamethoxazole and Trimethoprim Tablets, 400 mg/80 mg, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Amneal/Interpharm, NDC 53746-272-01
Reported: July 30, 2014 Initiated: September 27, 2011 #D-1450-2014
Product Description
Sulfamethoxazole and Trimethoprim Tablets, 800 mg/160 mg, DOUBLE STRENGTH, Rx, packaged and labeled to contain Sulfamethoxazole and Trimethoprim Tablets, 400 mg/80 mg, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Amneal/Interpharm, NDC 53746-272-01
Reason for Recall
Labeling: Label Mix up; product labeled to contain Sulfamethoxazole and Trimethoprim Tablets, 400 mg/80 mg instead of Sulfamethoxazole and Trimethoprim Tablets, 800 mg/160 mg
Details
- Recalling Firm
- Shamrock Medical Solutions Group LLC
- Units Affected
- 284/800 mg tablets
- Distribution
- Product was shipped to the following states: CO, MA, OH, TX & WY.
- Location
- Lewis Center, OH
Frequently Asked Questions
What product was recalled? ▼
Sulfamethoxazole and Trimethoprim Tablets, 800 mg/160 mg, DOUBLE STRENGTH, Rx, packaged and labeled to contain Sulfamethoxazole and Trimethoprim Tablets, 400 mg/80 mg, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Amneal/Interpharm, NDC 53746-272-01. Recalled by Shamrock Medical Solutions Group LLC. Units affected: 284/800 mg tablets.
Why was this product recalled? ▼
Labeling: Label Mix up; product labeled to contain Sulfamethoxazole and Trimethoprim Tablets, 400 mg/80 mg instead of Sulfamethoxazole and Trimethoprim Tablets, 800 mg/160 mg
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 30, 2014. Severity: Moderate. Recall number: D-1450-2014.
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