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

Is NDC 0143-1171-01 recalled?

Captopril · 100 TABLET in 1 BOTTLE (0143-1171-01)

Yes — this exact package was recalled

2 FDA recalls name the code 0143-1171-01 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
Captopril
Strength
CAPTOPRIL 12.5 mg/1
Form
Tablet · Oral
Labeler
Hikma Pharmaceuticals USA Inc.
Type
Human Prescription Drug
Product code
0143-1171

Recalls naming this package

Class II · Moderate risk

CapsuleTOPRIL

Labeling: Label Mixup: CapsuleTOPRIL, Tablet, 6.25 mg (1/2 of 12.5 mg) may have potentially been mislabeled as the following drug:, LUBIPROSTONE, Capsule, 24 mcg, NDC 64764024060, Pedigree: AD46312_1, EXP: 5/16/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-864-2014
Class II · Moderate risk

CapsuleTOPRIL

Labeling: Label Mixup: CapsuleTOPRIL, Tablet, 12.5 mg may have potentially been mislabeled as the following drug:, CALCITRIOL, Capsule, 0.25 mcg, NDC 00054000725, Pedigree: AD52778_13, EXP: 5/20/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-863-2014

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