Sandoz Inc recalls Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-co
See all recalls from Sandoz Inc →Recalled Product
Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (NDC 0781-5275-10), Rx only, Manufactured in India by Sandoz Private Ltd for Sandoz Inc., Princeton, NJ 08540.
Hazard / Issue
Subpotent Drug: out of specification results for assay test.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: a) FJ6599, Exp 05/17 and b) FJ6600, Exp 05/17
✅ 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 Donepezil Hydrochloride Tablets, 10 →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime