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

Is NDC 64980-0411-10 recalled?

Pregabalin · 1000 CAPSULE in 1 BOTTLE (64980-411-10)

Yes — this exact package was recalled

1 FDA recall names the code 64980-0411-10 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
Pregabalin
Strength
PREGABALIN 50 mg/1
Form
Capsule · Oral
Labeler
Rising Pharma Holdings, Inc.
Type
Human Prescription Drug · DEA CV
Product code
64980-0411

Recalls naming this package

Class III ยท Low risk

Pregabalin Capsules 50mg

Presence of Foreign Tablets/Capsules: Complaint received from a re-packager, American Health Packaging (AHP), where a foreign tablet was discovered in one of the bottles during packaging set up. Tablet identified as pantoprazole tablet 20mg.

Ongoing Particulate / foreign matter Rising Pharma Holding, Inc. NDC 64980-411-10 D-0541-2024

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