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

Is NDC 0603-5482-21 recalled?

Propranolol Hydrochloride · 100 TABLET in 1 BOTTLE (0603-5482-21)

Yes — this exact package was recalled

1 FDA recall names the code 0603-5482-21 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 10 mg/1
Form
Tablet · Oral
Labeler
Par Health USA, LLC
Type
Human Prescription Drug
Product code
0603-5482

Recalls naming this package

Class II · Moderate risk

Propranolol HCL

Labeling: Label Mixup: PROPRANOLOL HCL, Tablet, 10 mg may have potentially been mislabeled as one of the following drugs: LORazepam, Tablet, 0.25 mg (1/2 of 0.5 mg), NDC 00591024001, Pedigree: AD60243_1, EXP: 5/22/2014; PROPRANOLOL HCL, Tablet, 10 mg, NDC 23155011001, Pedigree: W003068, EXP: 6/12/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-993-2014

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