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

Is NDC 70518-0382-03 recalled?

Lisinopril and Hydrochlorothiazide

Yes — this exact package was recalled

1 FDA recall names the code 70518-0382-03 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
Lisinopril and Hydrochlorothiazide
Strength
HYDROCHLOROTHIAZIDE 12.5 mg/1; LISINOPRIL 20 mg/1
Form
Tablet · Oral
Labeler
Remedyrepack INC.
Type
Human Prescription Drug
Product code
70518-0382

Recalls naming this package

Class II ยท Moderate risk

Lisinopril/HCTZ 20mg/12.5mg Tablet

Presence of Foreign Tablets/Capsules: This is a spin-off recall of D-1581-2019 due to a product complaint where one of Lupin's Fenofibrate 145mg was observed in the 500 s count product bottle.

Terminated Particulate / foreign matter RemedyRepack Inc. NDC 68180-0519-02 D-1030-2020

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