FDAFDA · Food and drugs·Recall number D-0068-2022
Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10mg/240mg) , 10-count blister packs, Distributed By Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-5833-15
Published November 3, 2021 · Recall initiated: October 12, 2021
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
Failed Moisture Limits
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LORATADINE AND PSEUDOEPHEDRINE SULFATE
- Manufacturer
- SUN PHARMACEUTICAL INDUSTRIES INC
- Distributor
- Nationwide within the United States
- Lot
- Lot #: AC14635, Exp. Date 12/2022
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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