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

Is NDC 43598-0743-90 recalled?

Ezetimibe and Simvastatin · 90 TABLET in 1 BOTTLE (43598-743-90)

Yes — this exact package was recalled

1 FDA recall names the code 43598-0743-90 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
Ezetimibe and Simvastatin
Strength
EZETIMIBE 10 mg/1; SIMVASTATIN 40 mg/1
Form
Tablet · Oral
Labeler
Dr.Reddys Laboratories Inc
Type
Human Prescription Drug
Product code
43598-0743

Recalls naming this package

Class II · Moderate risk

Dr. Reddy's Ezetimibe and Simvastatin Tablets

Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in the bottle

Terminated Particulate / foreign matter Dr. Reddy's Laboratories, Inc. NDC 43598-743-05 D-0085-2022

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