23-05-2025
Indoco Remedies receives USFDA approval for Generic Allopurinol Tablets USP 200 mg
By Aman Shukla Published on May 23, 2025, 11:20 IST
Indoco Remedies Limited has received final approval from the United States Food and Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Allopurinol Tablets USP 200 mg. The approved product is a generic version of Zyloprim® 200 mg, originally marketed by Casper Pharma LLC.
Allopurinol is commonly prescribed to manage high levels of uric acid in the blood, a condition known as hyperuricemia. It is also used to control uric acid levels in patients undergoing cancer treatment or those with kidney stones, where elevated uric acid can cause further complications.
The approved product will be manufactured at Indoco Remedies' production facility located at L-14, Verna Industrial Area, Verna, Goa – 403722, India.
Aditi Panandikar, Managing Director, commented, 'Besides reflecting the capability of Indoco Remedies to deliver products of high-quality standards, this development also provides impetus to our growth aspirations in an important market such as the US.'
This approval allows Indoco Remedies to market Allopurinol Tablets USP 200 mg in the U.S. market, providing a therapeutic alternative for patients and contributing to the availability of cost-effective generic medications.
Aman Shukla is a post-graduate in mass communication . A media enthusiast who has a strong hold on communication ,content writing and copy writing. Aman is currently working as journalist at
