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

Is NDC 0228-2820-11 recalled?

Hydrochlorothiazide · 100 TABLET in 1 BOTTLE (0228-2820-11)

Yes — this exact package was recalled

1 FDA recall names the code 0228-2820-11 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
Hydrochlorothiazide
Strength
HYDROCHLOROTHIAZIDE 12.5 mg/1
Form
Tablet · Oral
Labeler
Actavis Pharma, Inc.
Type
Human Prescription Drug
Product code
0228-2820

Recalls naming this package

Class II · Moderate risk

Hydrochlorothiazide

Labeling: Label Mixup: HYDROCHLOROTHIAZIDE, Tablet, 12.5 mg may have potentially been mislabeled as one of the following drugs: hydrALAZINE HCl, Tablet, 100 mg, NDC 23155000401, Pedigree: AD73652_4, EXP: 5/29/2014; CLINDAMYCIN HCL, Capsule, 300 mg, NDC 00591312001, Pedigree: AD67989_1, EXP: 5/28/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-886-2014

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