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

Is NDC 0054-0007-25 recalled?

Calcitriol · 100 CAPSULE in 1 BOTTLE, PLASTIC (0054-0007-25)

Yes — this exact package was recalled

1 FDA recall names the code 0054-0007-25 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
Calcitriol
Strength
CALCITRIOL .25 ug/1
Form
Capsule · Oral
Labeler
Hikma Pharmaceuticals USA Inc.
Type
Human Prescription Drug
Product code
0054-0007

Recalls naming this package

Class II ยท Moderate risk

Calcitriol

Labeling: Label Mixup: CALCITRIOL, Capsule, 0.25 mcg may be potentially as one of the following drugs: ANAGRELIDE HCL, Capsule, 0.5 mg, NDC 00172524160, Pedigree: AD46414_7, EXP: 5/16/2014; BENAZEPRIL HCL, Tablet, 5 mg, NDC 65162075110, Pedigree: AD52778_7, EXP: 5/20/2014; CINACALCET HCL, Tablet, 30 mg, NDC 55513007330, Pedigree: W003615, EXP: 6/25/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-787-2014

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