Glenmark Pharmaceuticals Inc., based in New Jersey, has voluntarily recalled thousands of units of bisoprolol fumarate and ...

Glenmark Pharmaceuticals Inc. in Elmwood Park, N.J., is recalling the pills, which are in 2.5 mg and 6.25 mg doses.

The Food and Drug Administration (FDA) classified the recall with a Class lll risk level, suggesting that exposure to the ...

The FDA recalled multiple lots of blood pressure medication Ziac by Glenmark due to possible cross-contamination ...

The Food and Drug Administration has recalled a popular treatment for high blood pressure. The agency said that bottles of ...

A nationwide recall has been issued for bisoprolol fumarate and hydrochlorothiazide tablets after traces of the cholesterol ...

Traces of another heart-related drug may be inside this product from a major pharmaceutical manufacturer, reveals an FDA report.

The recall, announced on December 1 by the Food and Drug Administration (FDA), stems from testing that revealed traces of ezetimibe, a cholesterol-lowering medication also produced by Glenmark. The ...

Bisoprolol (Bebedol (5 mg)) is a beta- blocker, prescribed for heart disease.It relaxes blood vessels and slowing heart rate to improve and decrease blood pressure. The information provided on this ...

Glenmark Pharmaceuticals Ltd. has received the final approval by the United States Food & Drug Administration (U.S. FDA) for Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP, 2.5 mg/6.25 mg, 5 ...

This is a randomized, multicenter, parallel, open-label clinical study. The trial was performed in seven hospitals in China from December 2011 to April 2014. Key inclusion criteria included: (1) ...

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