
Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated April 29, 2024, titled "Glenmark Pharmaceuticals receives ANDA approval forAcetaminophen and Ibuprofen Tablets, 250 mg/125 mg (OTC)".
Filed with NSE · · 2 pages · English
Glenmark Pharmaceuticals Limited has received ANDA approval for Acetaminophen and Ibuprofen Tablets, which are over-the-counter medications. The approval was granted by the United States Food & Drug Administration, allowing Glenmark to distribute these tablets in the U.S. This product is bioequivalent to Advil® Dual Action with Acetaminophen Tablets, which has significant annual sales in the market. Glenmark's portfolio includes numerous products authorized for distribution in the U.S., with additional ANDAs pending approval.
Written by 6ix AI from the company’s filing. How 6ix writes summaries

Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated April 29, 2024, titled "Glenmark Pharmaceuticals receives ANDA approval forAcetaminophen and Ibuprofen Tablets, 250 mg/125 mg (OTC)".
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