Marksans Pharma's UK subsidiary, Relonchem Limited, has received Marketing Authorization from the UK MHRA for its Exemestane 25mg film-coated tablets, expanding the company's oncology product portfolio and strengthening its UK market presence.
Marksans Pharma Ltd has achieved a significant milestone as its wholly owned UK subsidiary, Relonchem Limited, received Marketing Authorization from the UK Medicines and Healthcare products Regulatory Agency (MHRA) for Exemestane 25mg film-coated tablets. This regulatory approval enables Relonchem to market and distribute this breast cancer treatment medication across the UK.
Key highlights include:
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The product authorized: Exemestane 25mg film-coated tablets, primarily used for treating estrogen receptor-positive breast cancer in postmenopausal women.
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Regulatory endorsement from the UK's MHRA, crucial for market introduction and compliance.
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Enhancement of Marksans Pharma’s oncology portfolio, supporting its strategy to expand in high-growth therapeutic segments.
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Strengthening of Marksans Pharma’s presence in the competitive UK pharmaceutical market through this authorization.
Marksans Pharma, headquartered in Mumbai with manufacturing facilities in India, the USA, and the UK, continues to grow its footprint globally. This latest MHRA approval aligns with the company’s focus on generic pharmaceuticals across key therapeutic areas including cardiovascular, central nervous system, anti-diabetic, pain management, and gastroenterological segments.
This authorization not only opens new market opportunities but also reinforces Marksans Pharma's position in international pharmaceutical markets, highlighting its regulatory competency and commitment to delivering vital treatments.
Source: Reuters, Marketscreener, Business Upturn, NSE India filings