Sandoz Incorporated recalls Amitriptyline HCl Tablets, USP 25 mg, Packaged in a)100-coun
See all recalls from Sandoz Incorporated →Recalled Product
Amitriptyline HCl Tablets, USP 25 mg, Packaged in a)100-count bottles (NDC 0781-1487-01) and b) 1000-count bottles ( NDC 0781-1487-10), Rx only, Manufactured by Sandoz Inc., Princeton, NJ 08540
Hazard / Issue
Cross Contamination With Other Product: Imipramine
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: a) GR3831, GS9690, Exp. 08/2019; b) GR3832, Exp. 08/2019.
✅ 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 Amitriptyline HCl Tablets, USP →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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