FDAFDA · Food and drugs·Recall number D-0049-2025
Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72
Published November 27, 2024 · Recall initiated: November 7, 2024
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurity/Degradation Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
- Distributor
- Nationwide within the United States
- Lot
- Lot #: C00128, Exp. Date 04/2025; C00146, Exp.Date 07/2025
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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