Drug recall D-0182-2020
Product
Dr. Reddy's Ranitidine Tablets, USP 150 mg, 24 count bottles, NDC 55111-404-34 (OTC)
Reason for recall
CGMP Deviations: Presence of NDMA impurity detected in product.
Lots and codes
Batch Numbers: All lots within expiry.
Recall details
- Recalling firm
- Dr. Reddy's Laboratories, Inc., Princeton, NJ
- Quantity
- N/A
- Distribution
- Product was distributed to major distributors throughout the United States who may have further distributed the product.
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 1, 2019
Related products
- Ranitidine – drug information
- NDC 55111-404 Ranitidine · Ranitidine Hydrochloride 150 mg/1 · Dr. Reddy's Laboratories Limited