Guaifenesin and Codeine Phosphate Oral Solution USP, 100mg/10 mg per 5 mL, 16 fl oz (473 ml) bottles, PAI Pharmaceutical Associates, Inc., Greenville, SC 29605, NDC 0121-0775-16
Reported: February 12, 2025 Initiated: January 7, 2025 #D-0222-2025
Product Description
Guaifenesin and Codeine Phosphate Oral Solution USP, 100mg/10 mg per 5 mL, 16 fl oz (473 ml) bottles, PAI Pharmaceutical Associates, Inc., Greenville, SC 29605, NDC 0121-0775-16
Reason for Recall
Superpotent; sodium benzoate preservative
Details
- Recalling Firm
- PAI Holdings, LLC. dba Pharmaceutical Associates Inc
- Units Affected
- 4080 Bottles
- Distribution
- OH
- Location
- Greenville, SC
Frequently Asked Questions
What product was recalled? ▼
Guaifenesin and Codeine Phosphate Oral Solution USP, 100mg/10 mg per 5 mL, 16 fl oz (473 ml) bottles, PAI Pharmaceutical Associates, Inc., Greenville, SC 29605, NDC 0121-0775-16. Recalled by PAI Holdings, LLC. dba Pharmaceutical Associates Inc. Units affected: 4080 Bottles.
Why was this product recalled? ▼
Superpotent; sodium benzoate preservative
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 12, 2025. Severity: Low. Recall number: D-0222-2025.
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