Glenmark Pharmaceuticals has initiated recall of 109,080 bottles of anti-inflammatory Indomethacin capsules (USP, 50 mg, 100-count bottle) from the US market, due to incorrect instructions on the labeling.
Glenmark’s current portfolio consists of 131 products authorized for distribution in the US marketplace and 63 ANDA’s pending approval with the US FDA. In addition to these internal filings, Glenmark continues to identify and explore external development partnerships to supplement and accelerate the growth of its existing pipeline and portfolio.