Reported Jul 27, 2022 · Terminated
Aripiprazole Tablets, USP 20 mg, packaged in a) 1,000-count bottle (NDC 60505-2676-8, UPC 3 60505 26768 2), b) 30-count…
Apotex Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Apotex Corp. · 2400 N Commerce Pkwy Ste 400 · Weston, FL · 33326-3253
Is this the product you have?
Aripiprazole TabletsUSP 20 mgpackaged in a) 1000-count bottle (NDC 60505-2676-8UPC 3 60505 26768 2)b) 30-count bottle (NDC 60505-2676-3UPC 3 60505 26763 7)Rx only
- Manufactured byApotex, Inc. Toronto
- Ontario Canada M9L 1T9 Manufactured forApotex Corp. Weston, Florida 33326
- Lot codes and dates
- Lots
a) TD9591 Exp. 04/2023b) TD9592 Exp. 04/2023
- Lots
- Amount recalled
- 2010 bottles
Where it was sold
- Nationwide
Why it was recalled
Failed dissolution specifications: OOS for dissolution at the 12-month stability time point.
This product could cause temporary or reversible health problems — stop using it.
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