FDAFDA · Food and drugs·Recall number D-0228-2018
Divalproex Sodium Delayed Release Tablets USP, 500 mg, 100-count bottle, RX Only, Manufactured by: Unichem Laboratories Ltd. Ind. Area, Meerut Road, Ghaziabad-201 003, India. Marketed By: Unichem Pharmaceuticals (USA), Inc. Hasbrouck Heights, NJ 07604. NDC 29300-140-01
Published January 24, 2018 · Recall initiated: December 19, 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
Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DIVALPROEX SODIUM
- Manufacturer
- Unichem Pharmaceuticals Usa Inc
- Distributor
- Product was distributed nationwide in the USA.
- UPC
- 0329300140019
- Lot
- Lot: ZDPH17040
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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