Apotex Corp. recalls Aripiprazole Tablets, USP 20 mg, packaged in a) 1,000-count
See all recalls from Apotex Corp. →Recalled Product
Aripiprazole Tablets, USP 20 mg, packaged in a) 1,000-count bottle (NDC 60505-2676-8, UPC 3 60505 26768 2), b) 30-count bottle (NDC 60505-2676-3, UPC 3 60505 26763 7), Rx only, Manufactured by: Apotex, Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326
Hazard / Issue
Failed dissolution specifications: OOS for dissolution at the 12-month stability time point.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lots: a) TD9591 Exp. 04/2023; b) TD9592 Exp. 04/2023
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Aripiprazole Tablets, USP 20 →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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