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

Is NDC 0904-6269-08 recalled?

Ziprasidone · 40 BLISTER PACK in 1 CARTON (0904-6269-08) / 1 CAPSULE in 1 BLISTER PACK

Yes — this exact package was recalled

1 FDA recall names the code 0904-6269-08 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
Ziprasidone
Strength
ZIPRASIDONE HYDROCHLORIDE 20 mg/1
Form
Capsule · Oral
Labeler
Major Pharmaceuticals
Type
Human Prescription Drug
Product code
0904-6269

Recalls naming this package

Class I ยท High risk

ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg

Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.

Terminated Labeling / mix-up The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories NDC 0904-6269-08 D-0893-2023

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