FDAFDA · Food and drugs·Recall number D-0940-2023
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.
Published August 2, 2023 · Recall initiated: July 13, 2023
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Foreign Substance: Metal embedded in a tablet.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- METHYLPHENIDATE HYDROCHLORIDE
- Manufacturer
- SUN PHARMACEUTICAL INDUSTRIES INC
- Distributor
- Nationwide
- UPC
- 0357664228883
- Lot
- Lot AC74459, Exp 07/31/2024
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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