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Aurobindo Pharma USA, Inc. Initiates Voluntary Nationwide Recall of Two (2) Lots of Quinapril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, Due to the Detection of N-Nitroso Quinapril Impurity. Summary: Risk Statement: Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables.
INDICATIONS AND USAGE: Hydrochlorothiazide tablets are indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cir rhosis, and corticosteroid and estrogen...
27 Οκτ 2022 · On Oct. 25, the U.S. Food and Drug Administration (FDA) announced a recall for two lots of Quinapril and Hydrochlorothiazide Tablets, USP 20mg/12.5mg by the drug manufacturer Aurobindo Pharma USA, Inc., due to a detection of Nitrosamine Drug Substance Related Impurity.
Pfizer will recall six lots of Accuretic tablets, one lot of quinapril and hydrochlorothiazide tablets and four lots of quinapril HCl/ hydrochlorothiazide tablets. Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables.
All Accuretic (quinapril hydrochloride and hydrochlorothiazide) tablets are being recalled at the pharmacy and wholesale level as a precautionary measure due to the observation of levels of...
This recall has been initiated as a precautionary measure due to the identification of a Clopidogrel tablet found in a bottle of the product. Unichem is requesting consumers who have the product that is being recalled to stop using it and return it to the place of purchase.
The recall is voluntary. It is for Hydrochlorothiazide 25 mg tablets. The FDA issued the recall due to a Clopidogrel tablet found in a bottle of the product. Our files show that you may have filled a prescription for this medicine. Please call your pharmacy to find out if your bottle could be part of this recall. The pharmacy may replace the drug.
