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

Is NDC 0781-1556-01 recalled?

Isosorbide Dinitrate · 100 TABLET in 1 BOTTLE (0781-1556-01)

Yes — this exact package was recalled

1 FDA recall names the code 0781-1556-01 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
Isosorbide Dinitrate
Strength
ISOSORBIDE DINITRATE 10 mg/1
Form
Tablet · Oral
Labeler
Sandoz Inc.
Type
Human Prescription Drug
Product code
0781-1556

Recalls naming this package

Class II · Moderate risk

Isosorbide Dinitrate

Labeling: Label Mixup: ISOSORBIDE DINITRATE, Tablet, 10 mg may have potentially been mislabeled as one of the following drugs: SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: AD22845_10, EXP: 5/2/2014; CALCITRIOL, Capsule, 0.5 mcg, NDC 63304024001, Pedigree: AD32757_10, EXP: 5/14/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-1000-2014

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