FDAFDA · Food and drugs·Recall number D-0797-2020
Preferred Pharmaceuticals, Inc, Ranitidine Tablets, 300 mg, Rx Only, a) 14 count bottles (NDC: 68788-6382-1), b) 30 count bottles (NDC: 68788-6382-3), c) 90 count bottles (NDC: 68788-6382-9), d) 100 count bottles (NDC: 68788-6382-0)
Published January 29, 2020 · Recall initiated: January 7, 2020
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
CGMP Deviations: Presence of NDMA impurity detected in product.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Preferred Pharmaceuticals, Inc
- Distributor
- Distribution to physicians in the following states: AL, AZ, CA, FL, GA, IN, and SC
- Lot
- Lot #: All lots within expiry
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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