Glenmark recalls 6,528 bottles of blood pressure drug in US
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Glenmark Pharmaceuticals is recalling 6,528 bottles of Diltiazem Hydrochloride extended-release capsules, a medication used to treat high blood pressure, in the US market. The recall is due to failed dissolution specifications in a long-term stability study. The affected lot, produced in India, is being recalled by Glenmark Pharmaceuticals Inc. The recall was initiated on March 26, 2024. India is the largest supplier of pharmaceuticals globally, with a 20% share in the global supply across 60 therapeutic categories.

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https://m.economictimes.com/industry/healthcare/biotech/pharmaceuticals/glenmark-recalls-6528-bottles-of-blood-pressure-drug-in-us/articleshow/109287094.cms