FDAFDA · Food and drugs·Recall number D-0101-2018
Paroxetine Tablets USP, 30 mg, a) 30 count (NDC 68382-099-06), b) 500 count (NDC 68382-099-05), and c) 1000 count (NDC 68382-099-10) count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534
Published December 6, 2017 · Recall initiated: November 20, 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: Risperidone Tablets were found in bottle of Paroxetine Tablets
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PAROXETINE
- Manufacturer
- Zydus Pharmaceuticals USA Inc
- Distributor
- Nationwide
- UPC
- 0368382098108
- Lot
- a) Z701308, b) Z701309, c) Z701310 exp April 2019
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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