Morepen Gets US FDA clearance for its Bulk Drug Montelukast Sodium
New Delhi , Dec 20 : The United States Food and Drug Administration (USFDA) has cleared Montelukast Sodium, a bulk drug / API manufactured by Morepen Laboratories Ltd., for sale in the US market. This gives Morepen an entry into the Rs. 2000 crore (Approx. USD 300 million) US market for Montelukast. The first commercial orders for the bulk drug are expected in Q2 of FY 2018-19.
Montelukast's global market is estimated at about Rs. 13000 crore (Approx. USD 2 billion) out of which US market alone is Rs. 2,000 crore. The patent for Montelukast has expired in all the markets worldwide. In U.S., the product patent got expired in 2012 and subsequently process patent expired in 2014.
Montelukast is another blockbuster product for Morepen after Loratadine. Morepen is amongst the largest producers of Montelukast globally with an annual capacity of more than 30 tons. Besides, Morepen is the market leader for Montelukast in India with over 50 per cent market share, supplying to almost all major finished dosage manufacturers in India. Already crossed Rs. 100 crore annual sales from Montelukast Sodium alone, Morepen is going to get a business of around Rs. 500 crore from this API in next three to four years.
Morepen holds process patent for Montelukast Sodium Amorphous for US, Canada and Europe markets. The company's manufacturing process yields very less impurities, very less residual solvents, higher assay, better color of the API and is an environment friendly process as it does not involve use of class II solvents.
Morepen's API Montelukast supplies are regular to various countries in Europe and also to China. Morepen also holds accreditations for other countries including Canada, Russia, Taiwan, Iran for Montelukast. Commercial sales of Montelukast are presently reaching customers in about 35 countries. U.S. supplies would also commence following the USFDA clearance.
Montelukast is manufactured at Morepen's Masulkhana facility, which has been inspected by various global regulatory agencies like US FDA, EU GMP, TGA and others. Montelukast is manufactured under strict quality control complying with cGMP requirements and meeting various other global manufacturing standards having already obtained COS (Certificate of Suitability) in Europe and IDL (Import Drug Licence) from China.
In the First Half (H1) of FY 2017-18, ended September 30, 2017, Morepen has reported a rise of 9 per cent in its net profit at Rs. 12.34 crore on its net sales of Rs. 257 crore. Morepen has also recently entered into a tie-up with Vesale Pharma International of Belgium to strengthen its position in the Rs. 1000 crore Probiotics market in India. (ANI-NewsVoir)