FDAFDA · Food and drugs·Recall number D-0237-2024
Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle, manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-626-90
Published January 24, 2024 · Recall initiated: December 29, 2023
Status when published: Ongoing — 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 Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- IBUPROFEN AND FAMOTIDINE
- Manufacturer
- Ascend Laboratories, LLC
- Distributor
- Nationwide
- Lot
- 23140190, Exp. Date 12/31/2024
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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