Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 64980-0221-01 recalled?

Methylphenidate Hydrochloride · 100 TABLET, CHEWABLE in 1 BOTTLE (64980-221-01)

Yes — this exact package was recalled

1 FDA recall names the code 64980-0221-01 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
Methylphenidate Hydrochloride
Strength
METHYLPHENIDATE HYDROCHLORIDE 2.5 mg/1
Form
Tablet, Chewable · Oral
Labeler
Rising Pharma Holdings, Inc.
Type
Human Prescription Drug · DEA CII
Product code
64980-0221

Recalls naming this package

Class II · Moderate risk

Methylphenidate Hydrochloride Chewable Tablets

Failed Tablet Specifications: Recall of this drug product was voluntarily initiated by the manufacturer due to a market complaint, which stated that a tablet in the sealed bottle was twice larger in size when compared to the remaining tablets. This complaint is second of its kind.

Ongoing Failed specification Rising Pharmaceuticals NDC 64980-221-01 D-0573-2022

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