Ranitidine Tablets, USP 75 mg, a.) 30 count bottles (NDC 69842-871-30) b.) 80 count bottles (NDC 69842-871-80) c.)160 count bottles (NDC 69842-871-37) (CVS) OTC

Recall Number: D-0173-2020

Firm: Dr. Reddy's Laboratories, Inc.

Classification: Class II

Status: Completed

Report Date: 20191113

Initiation Date: 20191001

Termination Date:

Reason for Recall

CGMP Deviations: Presence of NDMA impurity detected in product.

Product Description

Ranitidine Tablets, USP 75 mg, a.) 30 count bottles (NDC 69842-871-30) b.) 80 count bottles (NDC 69842-871-80) c.)160 count bottles (NDC 69842-871-37) (CVS) OTC