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

Is NDC 10702-0163-50 recalled?

Methylphenidate · 500 mL in 1 BOTTLE (10702-163-50)

Yes — this exact package was recalled

1 FDA recall names the code 10702-0163-50 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.

Active ingredient
Methylphenidate Hydrochloride
Strength
METHYLPHENIDATE HYDROCHLORIDE 5 mg/5mL
Form
Solution · Oral
Labeler
KVK-Tech, Inc.
Type
Human Prescription Drug · DEA CII
Product code
10702-0163

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