Class II · Moderate risk
Oxycodone and Acetaminophen CII Tablets USP
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
National Drug Code
Is NDC 0406-0523-01 recalled?
Oxycodone and Acetaminophen · 100 TABLET in 1 BOTTLE (0406-0523-01)
Yes — this exact package was recalled
1 FDA recall names the code 0406-0523-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- oxycodone hydrochloride and acetaminophen
- Strength
- OXYCODONE HYDROCHLORIDE 10 mg/1; ACETAMINOPHEN 325 mg/1
- Form
- Tablet · Oral
- Labeler
- SpecGx LLC
- Type
- Human Prescription Drug · DEA CII
- Product code
- 0406-0523
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
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