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

Is NDC 0591-0424-01 recalled?

Triamterene and Hydrochlorothiazide · 100 TABLET in 1 BOTTLE, PLASTIC (0591-0424-01)

Yes — this exact package was recalled

1 FDA recall names the code 0591-0424-01 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
Triamterene and Hydrochlorothiazide
Strength
TRIAMTERENE 37.5 mg/1; HYDROCHLOROTHIAZIDE 25 mg/1
Form
Tablet · Oral
Labeler
Actavis Pharma, Inc.
Type
Human Prescription Drug
Product code
0591-0424

Recalls naming this package

Class II · Moderate risk

Triamterene/ Hydrochlorothiazide

Labeling: Label Mixup: TRIAMTERENE/ HYDROCHLOROTHIAZIDE, Tablet, 37.5 mg/25 mg may have potentially been mislabeled as the following drug: SEVELAMER HCL, Tablet 800 mg, NDC 58468002101, Pedigree: W002858, EXP: 6/7/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-964-2014

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