Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 0378-0213-01 recalled?

Chlorthalidone · 100 TABLET in 1 BOTTLE (0378-0213-01)

Yes — this exact package was recalled

1 FDA recall names the code 0378-0213-01 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
chlorthalidone
Strength
CHLORTHALIDONE 50 mg/1
Form
Tablet · Oral
Labeler
Mylan Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
0378-0213

Recalls naming this package

Class II · Moderate risk

Chlorthalidone

Labeling: Label Mixup: CHLORTHALIDONE, Tablet, 50 mg may have potentially been mislabeled as the following drug: SENNOSIDES, Tablet, 8.6 mg, NDC 00182109301, Pedigree: W002979, EXP: 6/11/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-889-2014

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