Zydus receives final approval from USFDA for Colestipol Hydrochloride Tablets

Zydus receives final approval from USFDA for Nitroglycerin Sublingual Tablets Ahmedabad, India, 9 March, 2022 Zydus Lifesciences Ltd. has received final approval from the USFDA to market Nitroglycerin Sublingual Tablets in the strengths of 0.3 mg, 0.4mg and 0.6mg (US RLD: Nitrostat Sublingual Tablets). Nitroglycerin Sublingual Tablets are used to relieve chest pain (angina) in people who have a certain heart condition ( coronary artery disease). It may also be used before physical activities to help prevent chest pain. Nitroglycerin belongs to a class of drugs known as nitrates. Angina occurs when the heart muscle is not getting enoug h blood. This drug works by relaxing and widening blood vessels so blo od can flow more easily to the heart. The drug will be manufactured at the group’s formulation manufacturing facility at SEZ, Ahmedabad. The group now has 329 approvals and has so far filed over 400 ANDAs since the commencement of the filing process in FY 2003-04. About Zydus The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global lifesciences company that discovers, develops, manufactures, and markets a broad range of healthcare therapies. The group employs over 23000 people worldwide and is driven by its mission to unlock new possibilities in life - sciences through quality healthcare solutions that impact lives. The group aspires to transform lives through pathbreaking discoveries. For more details visit www.zyduslife.com. ***

The release as fetched from its publisher. zyduslife.com ↗