FDAFDA · Food and drugs·Recall number D-0928-2017
BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10
Published July 5, 2017 · Recall initiated: May 30, 2017
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 Moisture Limits: Product tested out-of-specification for moisture content.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Mckesson Packaging Services
- Distributor
- Nationwide in the US
- Lot
- Lot # 0113148, 0113149, 0113150, Exp: 04/18; 0113636, Exp: 06/18; 0114513, Exp: 10/18
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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