FDAFDA · Food and drugs·Recall number D-0914-2018
RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10
Published March 14, 2018 · Recall initiated: February 26, 2018
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 Stability Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Mckesson Packaging Services
- Distributor
- Nationwide
- Lot
- Lots: 0113064 Exp. 03/2018, 0114628 Exp. 08/2018, 0115189 Exp. 08/2018, 0115462 Exp. 09/2018
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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