Class II
Completed
Ranitidine Tablets, USP 150 mg, a.) 65 count bottles (NDC 49035-404-61) b.) 130 count bottles (NDC 49035-404-13) c.) 220 count bottles (NDC 49035-404-65) (Walmart) OTC
- Company
- Dr. Reddy'S Laboratories, Inc.
- Recall Initiated
- October 1, 2019
- Posted
- November 13, 2019
- Recall Number
- D-0171-2020
- Voluntary / Mandated
- Voluntary: Firm initiated
- Firm Location
- Princeton, NJ, United States
Reason for Recall
CGMP Deviations: Presence of NDMA impurity detected in product.
Distribution
Product was distributed to major distributors throughout the United States who may have further distributed the product.
Lot / Code Info
Batch Numbers: All lots within expiry.
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