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

Is NDC 55111-0629-30 recalled?

Eszopiclone · 30 TABLET, COATED in 1 BOTTLE (55111-629-30)

Yes — this exact package was recalled

1 FDA recall names the code 55111-0629-30 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.

1 of these recalls is still ongoing.

Active ingredient
Eszopiclone
Strength
ESZOPICLONE 1 mg/1
Form
Tablet, Coated · Oral
Labeler
Dr. Reddy's Laboratories Limited
Type
Human Prescription Drug · DEA CIV
Product code
55111-0629

Recalls naming this package

Class III ยท Low risk

Eszopiclone Tablets

Failed Impurities/Degradation Specifications: Related Substances

Ongoing Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-629-30 D-0581-2024

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