FDAFDA · Food and drugs·Recall number D-0147-2017
Amoxicillin for Oral suspension, USP 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: Hikma Pharmaceuticals, P.O. Box 183400, Amman 11118 - Jordan, NDC 0143-9887-01
Published November 30, 2016 · Recall initiated: November 4, 2016
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
Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- AMOXICILLIN
- Manufacturer
- West-Ward Pharmaceuticals Corp.
- Distributor
- Nationwide
- UPC
- 0301439887508
- Lot
- Lot #: AS1466A, Exp. Jan 2019
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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