Losartan oral tablet is a generic drug prescribed to treat high blood pressure, lower stroke risk in adults with high blood pressure and left ventricular hypertrophy, and treat diabetic nephropathy.

LOSARTAN POTASSIUM TAB, USP 50mg, 1000-count bottles, NDC number 13668-409-10, Lot 4O50C005, expiration date 11/2019. LOSARTAN POTASSIUM TAB, USP 25mg, 90-count bottles, NDC number 13668-113-90 ...

Losartan (Cozaar) is a generic drug that is prescribed for certain conditions, including high blood pressure. Losartan comes as an oral tablet and belongs to the angiotensin II receptor blocker ...

Torrent Pharmaceuticals Limited has again expanded a recall of its blood pressure medication over concerns the tablets contain small amounts of a cancer-causing ingredient. In a Sept. 19 statement ...

Macleods Pharmaceuticals Limited is recalling 32 lots of the popular blood pressure drug losartan after discovering trace amounts of a probable carcinogen. The recalled losartan and potassium ...

NATIONWIDE — The distributor of a variety of losartan, a popular blood pressure medication, has expanded the drug's recall over concerns it contains more than the acceptable trace amount of a ...

Torrent Pharmaceuticals Limited has once again expanded its recall of Losartan potassium tablets and Losartan potassium/hydrochlorothiazide tablets, the Food and Drug Administration announced ...

This covers lot No. JB8912 of Losartan Potassium Hydrochlorothiazide 100 mg or 25 mg tablets in 1,000-count bottles, expiration date 06/2020. None of the recalled tablets were distributed before ...

has approved its Abbreviated New Drug Application (ANDA) for Losartan Potassium and Hydrochlorothiazide Tablets USP, 50 mg/12.5 mg, 100 mg/12.5 mg, and 100 mg/25 mg. It is bioequivalent and ...

This study demonstrates that candesartan had greater efficacy in lowering arterial pressure when compared to losartan. Moreover, the duration of effect and response/control rates were ...

The recalled 100 mg/25 mg losartan and potassium/hydrochlorothiazide tablets contained small amounts of N-nitrosodiethylamine, or NDEA, according to a company recall notice shared on the Food and ...