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

Is NDC 45963-0557-50 recalled?

Gabapentin · 500 CAPSULE in 1 BOTTLE (45963-557-50)

Yes — this exact package was recalled

1 FDA recall names the code 45963-0557-50 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
Gabapentin
Strength
GABAPENTIN 400 mg/1
Form
Capsule · Oral
Labeler
Actavis Pharma, Inc.
Type
Human Prescription Drug
Product code
45963-0557

Recalls naming this package

Class II ยท Moderate risk

Gabapentin Capsules

Failed Capsule/Tablet Specifications: Actavis has received several complaint for clumping and breaking of capsules with some bottles showing popped out bottle bottom (round bottom) and creased labels from one distribution center.

Terminated Failed specification Actavis Elizabeth LLC NDC 14550-513-02 D-0336-2015

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