Business Standard

Alembic Pharma gains on USFDA nod for Mesalamine capsules

Image

Capital Market

Alembic Pharmaceuticals advanced 6.22% to Rs 614.45 after the drug maker received final approval from the US Food & Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Mesalamine extended-release capsules.

The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Apriso extended-release capsules of Salix Pharmaceuticals, Inc. (Salix).

Mesalamine extended-release capsules are indicated for the maintenance of remission of ulcerative colitis in adults.

According to IQVIA, Mesalamine extended-release capsules had an estimated market size of $133 million for twelve months ending June 2022.

Alembic Pharma has a cumulative total of 174 ANDA approvals (150 final approvals and 24 tentative approvals) from USFDA.

 

Alembic Pharmaceuticals is a vertically integrated research and development pharmaceutical company. It manufactures and markets generic pharmaceutical products all over the world.

The company reported a consolidated net loss of Rs 65.88 crore in Q1 FY23 as against a net profit of Rs 164.52 crore posted in Q1 FY22. Net sales fell 4.8% year on year to Rs 1,262.14 crore in the quarter ended 30 June 2022.

Powered by Capital Market - Live News

Disclaimer: No Business Standard Journalist was involved in creation of this content

Don't miss the most important news and views of the day. Get them on our Telegram channel

First Published: Nov 02 2022 | 12:28 PM IST

Explore News