Marksans Pharma Ltd’s subsidiary, Relonchem, has obtained UK Medicines and Healthcare products Regulatory Agency (MHRA) approval for its Mefenamic Acid Tablets. This regulatory milestone paves the way for expanded market access in the UK and signals growth opportunities within the pain management therapeutic area.
Marksans Pharma Ltd announced that its fully owned subsidiary, Relonchem, has received approval from the United Kingdom’s Medicines and Healthcare products Regulatory Agency (MHRA) for Mefenamic Acid Tablets. This approval is significant for strengthening Marksans Pharma’s international product portfolio and enhancing its presence in the competitive pain management market.
Key Highlights:
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Regulatory Approval: UK MHRA clearance for the manufacturing and marketing of Mefenamic Acid Tablets, used as an anti-inflammatory and analgesic medication.
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Market Expansion: The approval enables Relonchem to supply these tablets to the UK pharmaceutical market, aligning with the company’s global growth strategy.
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Product Application: Mefenamic Acid is widely prescribed for conditions including menstrual pain, musculoskeletal pain, and other inflammatory disorders, addressing unmet patient needs.
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Quality and Compliance: The approval reflects adherence to stringent MHRA standards for quality, safety, and efficacy.
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Strategic Implications: This regulatory success reinforces Marksans Pharma’s commitment to expanding its global footprint and diversifying its specialty pharmaceutical offerings.
The MHRA nod is a key step in consolidating Marksans Pharma’s position in international regulated markets and unlocking new growth avenues.
Sources: Marksans Pharma official release, UK MHRA regulatory announcements, Economic Times and Business Standard.