FDAFDA · Food and drugs·Recall number D-0631-2018
Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz, Inc., Princeton, NJ 08540, NDC 0781-5067-05.
Published April 25, 2018 · Recall initiated: April 6, 2018
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
Cross Contamination With Other Products: presence of unrelated ingredients (i.e. traces of Lisinopril, Mannitol, Iron, Calcium and Phosphorous).
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Sandoz Incorporated
- Distributor
- Nationwide in the USA and Puerto Rico
- Lot
- Lot #: GW8264, HD3095, Exp 12/18
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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