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

Is NDC 60429-0027-10 recalled?

Atenolol · 1000 TABLET in 1 BOTTLE, PLASTIC (60429-027-10)

Yes — this exact package was recalled

1 FDA recall names the code 60429-0027-10 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.

Active ingredient
atenolol
Strength
ATENOLOL 25 mg/1
Form
Tablet · Oral
Labeler
Golden State Medical Supply, Inc.
Type
Human Prescription Drug
Product code
60429-0027

Recalls naming this package

Class I ยท High risk

Atenolol Tablets

Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets

Terminated Labeling / mix-up Golden State Medical Supply Inc. NDC 60429-027-10 D-0019-2023

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