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

Is NDC 0054-0088-26 recalled?

Calcium Acetate · 200 CAPSULE in 1 BOTTLE (0054-0088-26)

Yes — this exact package was recalled

1 FDA recall names the code 0054-0088-26 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
Calcium Acetate
Strength
CALCIUM ACETATE 667 mg/1
Form
Capsule · Oral
Labeler
Hikma Pharmaceuticals USA Inc.
Type
Human Prescription Drug
Product code
0054-0088

Recalls naming this package

Class II · Moderate risk

Calcium Acetate

Labeling: Label Mixup: CALCIUM ACETATE, Capsule, 667 mg may be potentially mislabeled as one of the following drugs: ZOLPIDEM TARTRATE, Tablet, 2.5 mg (1/2 of 5 mg), NDC 64679071401, Pedigree: AD28355_1, EXP: 5/8/2014; acetaZOLAMIDE, Tablet, 250 mg, NDC 51672402301, Pedigree: AD62865_1, EXP: 5/23/2014; ZINC GLUCONATE, Tablet, 50 mg, NDC 00904319160, Pedigree: W003028, EXP: 6/12/2014; PROPRANO

Terminated Labeling / mix-up Aidapak Services, LLC D-794-2014

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