Class II · Moderate risk
Tacrolimus Capsules
Cross Contamination with Other Products: findings of carryover of trace amounts of a previously manufactured product fluvastatin
National Drug Code
Is NDC 0781-2102-01 recalled?
Tacrolimus · 100 CAPSULE in 1 BOTTLE (0781-2102-01)
Yes — this exact package was recalled
2 FDA recalls name the code 0781-2102-01 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 .5 mg/1
- Form
- Capsule · Oral
- Labeler
- Sandoz Inc.
- Type
- Human Prescription Drug
- Product code
- 0781-2102
Recalls naming this package
Class II · Moderate risk
Tacrolimus
Labeling: Label Mixup: TACROLIMUS, Capsule, 0.5 mg may have potentially been mislabeled as one of the following drugs: CINACALCET HCL, Tablet, 30 mg, NDC 55513007330, Pedigree: W003168, EXP: 6/13/2014; ISOSORBIDE MONONITRATE ER, Tablet, 30 mg, NDC 62175012837, Pedigree: W003350, EXP: 6/18/2014.
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
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