Marksans Pharma gets USFDA approval for Esomeprazole Magnesium delayed-release capsules

Marksans Pharma gets USFDA approval for Esomeprazole Magnesium delayed-release capsules

By: IPP Bureau

Last updated : October 05, 2023 11:03 am



This product is bioequivalent to the reference listed drug (RLD), Nexium 24 HR Delayed- Release Capsules, 2.0mg (OTC), of AstraZeneca Pharmaceuticals


Marksans Pharma Limited has received final approval from US Food & Drugs Administration for its Abbreviated New' Drug Application (ANDA) for Esomeprazole Magnesium Delayed-Release Capsules USP, 20 mg (OTC).

This product is bioequivalent to the reference listed drug (RLD), Nexium 24 HR Delayed- Release Capsules, 2.0mg (OTC), of AstraZeneca Pharmaceuticals LP.

Esomeprazole is used to treat certain stomach and esophagus problems. It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as heartburn, difficulty swallowing, and cough. This medication helps heal acid damage to the stomach and esophagus, helps prevent ulcers and is expected to help prevent cancer of the esophagus. Esomeprazole belongs to a class of drugs known as proton pump inhibitors (PPIs).

The product will be manufactured at the company's formulation manufacturing facility in Goa, India.

Marksans Pharma USFDA AstraZeneca Pharmaceuticals

First Published : October 05, 2023 12:00 am