Class II · ModerateRecall completed
Nadolol Tablets
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot GG1539
Where it was soldMS and OH.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Failed dissolution specification: recalled due to an out of specification dissolution result of 40% (Specification: NLT 80%)
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made bySandoz Inc., Princeton, NJ 08540
| Distributed by / for | Sandoz Incorporated |
| NDC | 0781-1182-10 |
Show the full FDA record
| Full product label | Nadolol Tablets, USP, 40mg, packaged in 1000-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0781-1182-10 |
| Recalling firm | Sandoz Incorporated |
| Distribution | MS and OH. |
| Quantity | 96 bottles |
| Recall initiated | 2016-12-22 |
| Report date | 2017-01-04 |
| Recall completed | 2017-09-18 |
| Recall number | D-0236-2017 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Broomfield CO United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.