Class II · Moderate risk
Actoplus met XR
Defective Delivery System: tablets may be missing, in whole or in part, the laser drilled holes on the metformin core of the Actoplus met XR tablets.
National Drug Code
Is NDC 64764-0510-30 recalled?
Actoplus met XR
Yes — this exact package was recalled
1 FDA recall names the code 64764-0510-30 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 64764-0080 Amitiza 2
- 64764-0119 See recall 2
- 64764-0240 Amitiza 2
- 64764-0890 See recall 1
- 64764-0918 Uloric 1
Free recall alerts
Know the day your medication is recalled
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