Ahmedabad: Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration (US FDA) to market Febuxostat Tablets, 40 mg and 80 mg (USRLD: Uloric Tablets).

Indoco Remedies on Tuesday said it has got final approval from the US health regulator for Febuxostat tablets used for the treatment of gout caused by excessive levels of uric acid in the blood. The ...

Drug firm Alembic Pharmaceuticals Tuesday said it has received approval from the US health regulator for Febuxostat tablets, used to lower high levels of uric acid in adults who have gout. The ...

Global pharma major Lupin Limited (Lupin) on Thursday announced that it has received approval from the United States Food and Drug Administration (U.S. FDA) for its Abbreviated New Drug Application ...

HYDERABAD, India & PRINCETON, N.J.--(BUSINESS WIRE)--Dr. Reddy’s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY, along with its subsidiaries together referred to as “Dr.

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Febuxostat (Goustat (80 mg)) is a xanthine oxidase (XO) inhibitor, prescribed for gout and hyperuricemia (high level of uric acid in blood). It decreases the amount of uric acid in blood. The ...

New Delhi: Indoco Remedies on Tuesday said it has got final approval from the US health regulator for Febuxostat tablets used for the treatment of gout caused by excessive levels of uric acid in the ...

HYDERABAD, India & PRINCETON, N.J.--(BUSINESS WIRE)-- Dr. Reddy’s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY, along with its subsidiaries together referred to as “Dr.

Alembic Pharmaceuticals has received tentative approval from the US health regulator for Febuxostat tablets used for treatment of hyperuricemia in patients of gout. "The company has received tentative ...