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

Is NDC 0228-2778-11 recalled?

Propranolol Hydrochloride · 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2778-11)

Yes — this exact package was recalled

1 FDA recall names the code 0228-2778-11 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
Propranolol Hydrochloride
Strength
PROPRANOLOL HYDROCHLORIDE 60 mg/1
Form
Capsule, Extended Release · Oral
Labeler
Actavis Pharma, Inc.
Type
Human Prescription Drug
Product code
0228-2778

Recalls naming this package

Class II · Moderate risk

Propranolol HCL ER

Labeling: Label Mixup: PROPRANOLOL HCL ER, Capsule, 60 mg may have potentially been mislabeled as the following drug: CINACALCET HCL, Tablet, 30 mg, NDC 55513007330, Pedigree: AD52778_82, EXP: 5/21/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-885-2014

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