Drug recall D-0940-2023
Product
Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, NDC 57664-230-88.
Reason for recall
Presence of Foreign Substance: Metal embedded in a tablet.
Lots and codes
Lot AC74459, Exp 07/31/2024
Recall details
- Recalling firm
- SUN PHARMACEUTICAL INDUSTRIES INC, Princeton, NJ
- Quantity
- 7313 bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 13, 2023
- Terminated
- February 12, 2024
Related products
- Methylphenidate Hydrochloride – drug information
- NDC 57664-230 Methylphenidate Hydrochloride · Methylphenidate Hydrochloride 20 mg/1 · Sun Pharmaceutical Industries, Inc.
- NDC 57664-229 Methylphenidate Hydrochloride · Methylphenidate Hydrochloride 10 mg/1 · Sun Pharmaceutical Industries, Inc.
- NDC 57664-228 Methylphenidate Hydrochloride · Methylphenidate Hydrochloride 5 mg/1 · Sun Pharmaceutical Industries, Inc.