Drug recall D-1473-2022
Product
Neomycin Sulfate Tablets, USP 500 mg , 100-count bottles, Rx only, Distributed by: TEVA PHARMACEUTICALS USA, INC North Wales, PA 19454, NDC 0093-1177-01
Reason for recall
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.
Lots and codes
Lot #: 3007830, 3007746, 3007829, Exp. Date 10/2024
Recall details
- Recalling firm
- Teva Pharmaceuticals USA Inc, Parsippany, NJ
- Distribution
- Nationwide within the United States
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 23, 2022
- Terminated
- September 7, 2023
Related products
- Neomycin Sulfate – drug information
- NDC 0093-1177 Neomycin Sulfate · Neomycin Sulfate 500 mg/1 · Teva Pharmaceuticals USA, Inc.