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

Is NDC 55111-0671-31 recalled?

Clopidogrel bisulfate · 5 BLISTER PACK in 1 CARTON (55111-671-31) / 6 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-06)

Yes — this exact package was recalled

2 FDA recalls name the code 55111-0671-31 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
Clopidogrel bisulfate
Strength
CLOPIDOGREL BISULFATE 300 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Dr.Reddy's Laboratories Limited
Type
Human Prescription Drug
Product code
55111-0671

Recalls naming this package

Class II · Moderate risk

Clopidogrel Tablets

Failed dissolution specification -Two additional lots being recalled due to Out-of-Specification results observed for dissolution at 18th month stability testing.

Terminated Dissolution failure Dr. Reddy's Laboratories, Inc. NDC 55111-671-31 D-0294-2019
Class II · Moderate risk

Clopidogrel Tablets

Failed Dissolution Specification: Out-of-Specification results were observed for dissolution at 18th month stability testing.

Terminated Dissolution failure Dr. Reddy's Laboratories, Inc. NDC 55111-671-31 D-0283-2019

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