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

Is NDC 0781-2103-01 recalled?

Tacrolimus · 100 CAPSULE in 1 BOTTLE (0781-2103-01)

Yes — this exact package was recalled

1 FDA recall names the code 0781-2103-01 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
Tacrolimus
Strength
TACROLIMUS 1 mg/1
Form
Capsule · Oral
Labeler
Sandoz Inc.
Type
Human Prescription Drug
Product code
0781-2103

Recalls naming this package

Class II ยท Moderate risk

Tacrolimus

Labeling: Label Mixup: TACROLIMUS, Capsule, 1 mg may have potentially been mislabeled as one of the following drugs: BISOPROLOL FUMARATE, Tablet, 5 mg, NDC 29300012601, Pedigree: AD34934_7, EXP: 5/10/2014; SEVELAMER CARBONATE, Tablet, 800 mg, NDC 58468013001, Pedigree: AD56917_4, EXP: 5/21/2014; SEVELAMER CARBONATE, Tablet, 800 mg, NDC 58468013001, Pedigree: AD73627_11, EXP: 5/30/2014; ATOMOXE

Terminated Labeling / mix-up Aidapak Services, LLC D-1007-2014

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