FDAFDA · Food and drugs·Recall number D-0605-2017
ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534.
Published March 29, 2017 · Recall initiated: March 6, 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
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ATENOLOL
- Manufacturer
- Zydus Pharmaceuticals USA Inc
- Distributor
- Nationwide in the USA and Puerto Rico.
- Lot
- Lot #: a) Z600724, Exp 04/18; Z600725, Exp 04/18
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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