Marksans Pharma's UK Subsidiary Secures Approval for Clonidine Tablets

1 min read     Updated on 15 Oct 2025, 02:02 PM
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Shriram ShekharScanX News Team
Overview

Marksans Pharma's wholly-owned UK subsidiary, Relonchem Limited, has received Marketing Authorization from the UK Medicines and Healthcare products Regulatory Agency (MHRA) for two Clonidine tablet products. The approval covers Clonidine Tablets (100 microgram) and Clonidine Hydrochloride Tablets (25 microgram). This development allows Marksans Pharma to expand its product offerings in the UK pharmaceutical market, potentially boosting its growth in the European sector.

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*this image is generated using AI for illustrative purposes only.

Marksans Pharma Limited, a prominent player in the pharmaceutical industry, has announced a significant development for its UK operations. The company's wholly-owned subsidiary, Relonchem Limited, has received Marketing Authorization from the UK Medicines and Healthcare products Regulatory Agency (MHRA) for two key products:

Product Approvals

Product Strength
Clonidine Tablets 100 microgram
Clonidine Hydrochloride Tablets 25 microgram

This regulatory approval marks an important milestone for Marksans Pharma, as it allows the company to expand its product offerings in the UK pharmaceutical market. Clonidine, the active ingredient in both approved formulations, is commonly used to treat high blood pressure and has other medical applications.

Company Overview

Marksans Pharma Limited, headquartered in Mumbai, India, is a global pharmaceutical company engaged in the research, manufacturing, and marketing of generic pharmaceutical formulations. The company's operations span multiple countries, with manufacturing facilities in India, the USA, and the UK.

Strategic Implications

The approval of these Clonidine products strengthens Marksans Pharma's position in the UK market and aligns with the company's strategy of expanding its global footprint. This development is expected to contribute to the company's growth in the European pharmaceutical sector.

Regulatory Compliance

It's worth noting that Marksans Pharma's manufacturing facilities have received approvals from several leading regulatory agencies, including:

  • U.S. Food and Drug Administration (USFDA)
  • UK Medicines and Healthcare products Regulatory Agency (MHRA)
  • Australian Therapeutic Goods Administration (TGA)

These approvals underscore the company's commitment to maintaining high quality standards in its pharmaceutical production.

The marketing authorization for Clonidine tablets represents a positive step for Marksans Pharma's UK subsidiary, potentially opening up new revenue streams and reinforcing the company's presence in the competitive pharmaceutical landscape.

Historical Stock Returns for Marksans Pharma

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Marksans Pharma's UK Arm Secures Approval for Moxonidine Tablets

1 min read     Updated on 23 Sept 2025, 02:16 PM
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Reviewed by
Naman SharmaScanX News Team
Overview

Marksans Pharma's wholly-owned UK subsidiary, Relonchem Limited, has obtained Marketing Authorization from the UK Medicines and Healthcare products Regulatory Agency (MHRA) for Moxonidine 200 microgram and 400 microgram Tablets. Moxonidine is used to treat mild to moderate essential hypertension. This approval allows Relonchem to market these products in the UK, potentially expanding Marksans Pharma's presence in the cardiovascular therapeutic segment. The authorization aligns with the company's strategy to strengthen its global generic pharmaceutical portfolio.

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*this image is generated using AI for illustrative purposes only.

Marksans Pharma announced a significant development for its UK operations. The company's wholly-owned subsidiary, Relonchem Limited, has received Marketing Authorization from the UK Medicines and Healthcare products Regulatory Agency (MHRA) for two key products: Moxonidine 200 microgram Tablets and Moxonidine 400 microgram Tablets.

Regulatory Milestone

This regulatory approval marks an important step for Marksans Pharma's presence in the UK pharmaceutical market. Moxonidine, the active ingredient in these newly approved tablets, is primarily used for the treatment of mild to moderate essential hypertension. The authorization allows Relonchem Limited to market these pharmaceutical products in the UK, potentially expanding Marksans Pharma's footprint in the cardiovascular therapeutic segment.

Strategic Implications

The approval aligns with Marksans Pharma's strategy to strengthen its global generic pharmaceutical portfolio. With manufacturing facilities approved by leading regulatory agencies, including the USFDA, UKMHRA, and Australian TGA, this new authorization further solidifies the company's position in regulated markets.

Company Profile

Marksans Pharma Limited, headquartered in Mumbai, India, is engaged in the research, manufacturing, and marketing of generic pharmaceutical formulations in global markets. The company's product portfolio spans major therapeutic segments, including cardiovascular system (CVS), central nervous system (CNS), anti-diabetic, pain management, gastroenterological, and anti-allergies.

Investor Relations

In related news, Marksans Pharma has scheduled an investor/analyst conference for September 23, 2025, at 10:00 AM IST. The physical meeting, part of the Pharma & Healthcare Conference by DAM Capital, will be held at Trident BKC. This event underscores the company's commitment to maintaining transparent communication with its stakeholders.

As Marksans Pharma continues to expand its product offerings and market presence, this latest approval for Moxonidine tablets represents another step in the company's growth strategy in the competitive global pharmaceutical landscape.

Historical Stock Returns for Marksans Pharma

1 Day5 Days1 Month6 Months1 Year5 Years
-1.01%-0.20%+3.89%-22.63%-34.85%+239.81%
Marksans Pharma
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