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

Is NDC 55111-0123-05 recalled?

Atorvastatin Calcium · 500 TABLET in 1 BOTTLE (55111-123-05)

Yes — this exact package was recalled

4 FDA recalls name the code 55111-0123-05 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 40 mg/1
Form
Tablet · Oral
Labeler
Dr. Reddy's Laboratories Limited
Type
Human Prescription Drug
Product code
55111-0123

Recalls naming this package

Class III · Low risk

Atorvastatin Calcium Tablets

Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and FP, Dihydroxy epoxy and Dieto epoxy impurities

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-123-90 D-0291-2021
Class III · Low risk

Atorvastatin Calcium tablets

Failed Impurities/Degradation Specifications - OOS was observed for ATV Cyclo FP Impurity and Total Degradation Impurities tested at the 18 month stability time point in Atorvastatin Calcium Tablets 40 mg 500 tablets.

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-123-05 D-1079-2018
Class III · Low risk

Atorvastatin Calcium Tablets 40 mg

Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-123-05 D-0420-2018

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