Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 64950-0354 recalled?

Oxycodone Hydrochloride

This product was recalled — in other package sizes

No FDA recall names your exact package code, but 1 recall cover the same product (64950-0354) in a different bottle or carton size. Worth checking with your pharmacist.

Active ingredient
Oxycodone Hydrochloride
Strength
OXYCODONE HYDROCHLORIDE 5 mg/5mL
Form
Solution · Oral
Labeler
Genus Lifesciences Inc.
Type
Human Prescription Drug · DEA CII
Product code
64950-0354

Recalls of this product

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.