FDAFDA · Food and drugs·Recall number D-1500-2014
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC # 59746-339-90
Published August 6, 2014 · Recall initiated: July 11, 2014
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: Tablets may contain dark blemishes identified as stainless steel.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Brand
- LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
- Manufacturer
- Jubilant Cadista Pharmaceuticals Inc.
- Distributor
- Nationwide and Puerto Rico
- UPC
- 0359746338107
- Lot
- Lot #14P0292, Exp 04/2016
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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