Glenmark Receives US FDA Approval for Acetaminophen and Ibuprofen Tablets

Glenmark Receives US FDA Approval for Acetaminophen and Ibuprofen Tablets

By, Admin 30 April 2024

"Glenmark Pharma receives US FDA approval for acetaminophen and ibuprofen tablets, 250 mg/125 mg

Overview

Glenmark Pharmaceuticals Ltd. (Glenmark), a research-led, global pharmaceutical company, has received final approval by the United States Food & Drug Administration (FDA) for acetaminophen and ibuprofen tablets, 250 mg/125 mg (OTC), determined by the FDA to be bioequivalent to Advil dual action with acetaminophen tablets, 250 mg/125 mg (OTC), of Haleon US Holdings, LLC.
 
Glenmark’s acetaminophen and ibuprofen tablets, 250 mg/125 mg (OTC), will be distributed in the US by Glenmark Therapeutics Inc., USA. 

Annual Sales

According to Nielsen syndicated data for the latest 52 weeks period ending March 23, 2024, the Advil dual action with acetaminophen tablets, 250 mg/125 mg (OTC) market achieved annual sales of approximately $84.1 million. 

Current Portfolio

  • Glenmark’s current portfolio consists of 195 products authorized for distribution in the US marketplace and 52 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.

Glenmark Pharmaceuticals

  • Glenmark Pharmaceuticals Ltd. is a research-led, global pharmaceutical company, having a presence across branded, generics, and OTC segments; with a focus on therapeutic areas of respiratory, dermatology and oncology. 
  • The company has 11 world-class manufacturing facilities spread across 4 continents, and operations in over 80 countries.

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