Glenmark Pharmaceuticals recalls 6,528 US bottles of high blood pressure drug Diltiazem Hydrochloride due to failed dissolution standards, per the US FDA.
Glenmark Pharmaceuticals recalls 6,528 bottles of a high blood pressure medication in the US market due to failed dissolution specifications, according to the US Food and Drug Administration (FDA). The affected lot of Diltiazem Hydrochloride extended-release capsules, produced in India, is being recalled by New Jersey-based Glenmark Pharmaceuticals Inc. The Class II recall was initiated on March 26.
April 14, 2024
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