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

Is NDC 55111-0124-90 recalled?

Atorvastatin Calcium · 90 TABLET in 1 BOTTLE (55111-124-90)

Yes — this exact package was recalled

2 FDA recalls name the code 55111-0124-90 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
Atorvastatin Calcium
Strength
ATORVASTATIN CALCIUM TRIHYDRATE 80 mg/1
Form
Tablet · Oral
Labeler
Dr. Reddy's Laboratories Limited
Type
Human Prescription Drug
Product code
55111-0124

Recalls naming this package

Class III · Low risk

Atorvstatin Calcium Tablets

Failed Impurities/Degradation Specifications: Out of Specification results for related substance.

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-124-90 D-0726-2022
Class II · Moderate risk

Atorvastatin Calcium Tablets

Presence of Foreign Substance: A product complaint was received for a defective tablet with an embedded foreign object observed in a bottle.

Terminated Particulate / foreign matter Dr. Reddy's Laboratories, Inc. NDC 55111-124-90 D-0878-2018

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