Senores Pharma Acquires Apnar Pharma in Deal Worth ₹91 Crores

3 min read     Updated on 15 Dec 2025, 07:55 PM
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Reviewed by
Riya DScanX News Team
Overview

Senores Pharmaceuticals has announced the acquisition of Apnar Pharma Private Limited for ₹91 crores, providing immediate access to regulated markets including US, UK, and Canada through an USFDA-approved manufacturing facility in Gujarat. The deal includes 5 ANDAs with a total addressable market of $722 million and significant production capacity across multiple dosage forms. The acquisition will be completed in two tranches by Q2 FY2027, with strategic benefits including enhanced market access, operational synergies, and strengthened CDMO capabilities.

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Senores Pharmaceuticals Limited has announced a strategic acquisition that will expand its pharmaceutical manufacturing capabilities. The company's Management Committee of the Board of Directors approved the acquisition of Apnar Pharma Private Limited on December 15, 2025, marking a significant step in the company's growth strategy.

Acquisition Structure and Timeline

Senores Pharmaceuticals has announced the acquisition of a 100% stake in Apnar Pharma Private Limited for a total enterprise value of ₹91.00 crores. The acquisition will be completed in two tranches by Q2 FY2027, with Apnar Pharma becoming a wholly owned subsidiary upon completion.

Parameter: Details
Total Enterprise Value: ₹91.00 crores
First Tranche: 75% by March 2026
Second Tranche: 25% by Q2 FY2027
Shareholding Acquired: 100%

Financial Structure

The deal structure combines cash payments with debt and liability assumptions, providing a balanced approach to the acquisition financing. The total consideration reflects the strategic value of acquiring established pharmaceutical manufacturing capabilities.

Component: Amount
Debt and Liabilities: ₹76.00 crores
Cash Payment: ₹15.00 crores
Payment Structure: Two tranches (75% and 25%)

Manufacturing Facility Specifications

The acquired facility in Jambusar, Gujarat represents a state-of-the-art pharmaceutical manufacturing operation that commenced in 2021. The facility received USFDA approval in September 2022 and maintains multiple international regulatory certifications.

Facility Parameter: Details
Total Land Area: 49,250 Sq. Mts (2 land parcels)
Construction Area: 40,000 Sq. Ft on 4,500 Sq. Mts
Employee Strength: 504 employees
Approved ANDAs: 5 ANDAs/15 Strengths
Total Addressable Market: $722 million

Production Capacity and Market Reach

The facility demonstrates significant production capabilities across multiple dosage forms with expansion potential. Current operations serve regulated markets including the US, UK, and Canada.

Product Category: Annual Capacity Expandable Capacity
Tablets: 275 million units 600 million units
Capsules: 225 million units 500 million units
Bottles: 16 million units 32 million units

Target Company Profile

Apnar Pharma Private Limited brings significant manufacturing credentials to the acquisition. The company was incorporated in Gujarat on December 12, 2014, under the Companies Act, 2013, and has established itself as a manufacturer of generic pharmaceutical formulations.

Key operational highlights include:

  • USFDA approved manufacturing facility
  • UK-MHRA certification
  • Health Canada approval
  • Manufacturing facility located in Jambusar, Gujarat
  • Focus on generic pharmaceutical formulations
  • Strong R&D and analytical capabilities

Financial Performance Track Record

Apnar Pharma's revenue performance over the past three years demonstrates the operational scale of the acquisition target.

Year: Turnover (₹ Lakhs)
March 2023: 1,575.16
March 2024: 2,756.26
March 2025: 1,421.88

Strategic Rationale and Synergies

The acquisition provides immediate access to regulated markets including UK and Canada, expanding beyond Senores Pharmaceuticals' current US presence. The deal includes 5 approved ANDAs representing a total market opportunity exceeding $700 million.

According to Swapnil Shah, Promoter Managing Director, the acquisition will enable the company to manufacture select US products from India, improving operational leverage and supporting margin expansion. The facility will strengthen manufacturing capabilities and deepen customer relationships, creating opportunities in the CDMO and CMO segments.

Key strategic benefits include:

  • Enhanced market access across regulated territories
  • Revenue and cost synergies through cross-selling
  • Backward integration via in-house manufacturing
  • Improved supply chain control and regulatory compliance
  • Expansion of product portfolio and customer penetration

ANDA Portfolio Acquisition

In addition to the facility acquisition, Senores Pharmaceuticals Inc., the company's wholly owned subsidiary, is acquiring a basket of 5 ANDAs from Apnar Pharma's parent company. Of these 5 ANDAs, 3 are validated and qualified, with commercialization expected to begin immediately.

The transaction has been disclosed under Regulation 30 of the Securities and Exchange Board of India (Listing Obligations and Disclosure Requirements) Regulations, 2015, ensuring full compliance with regulatory requirements.

Historical Stock Returns for Senores Pharmaceuticals

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Senores Pharmaceuticals Launches Deferiprone Tablets in US Through Dr. Reddy's Partnership

2 min read     Updated on 11 Dec 2025, 09:39 PM
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Reviewed by
Shriram SScanX News Team
Overview

Senores Pharmaceuticals has received regulatory approval and launched Deferiprone Tablets USP in 500mg and 1000mg strengths for the US market. The product, bioequivalent to Chiesi USA's Ferriprox Tablets, will be marketed by Dr. Reddy's Laboratories Inc. The market size for Deferiprone Tablets is approximately $70 million MAT. This launch aligns with Senores' strategy to enter niche, limited-competition generic formulations. The company has a portfolio of 46 ANDAs with 133 strengths and operates manufacturing facilities in the US and India.

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

Senores Pharmaceuticals has announced the regulatory approval and commercial launch of Deferiprone Tablets USP in 500mg and 1000mg strengths for the United States market. The pharmaceutical company disclosed this development through a media release filed under Regulation 30 of SEBI listing requirements.

Product Launch and Market Partnership

The newly launched Deferiprone Tablets are bioequivalent and therapeutically equivalent to Ferriprox Tablets manufactured by Chiesi USA, Inc. The product will be marketed and distributed by Dr. Reddy's Laboratories Inc. in the US market, representing a strategic partnership for market penetration.

Parameter Details
Product Deferiprone Tablets USP
Strengths 500mg and 1000mg
Reference Product Ferriprox Tablets (Chiesi USA)
Marketing Partner Dr. Reddy's Laboratories Inc.
Market Size $70.00 million MAT

Market Opportunity and Strategic Focus

According to Symphony data, Deferiprone Tablets in both brand and generic forms generated approximately $70.00 million in US sales for the twelve months ending in recent data. Swapnil Shah, Managing Director of Senores Pharmaceuticals Limited, emphasized the strategic importance of this launch, stating it advances the company's growth through entry into a limited-competition product segment.

The launch aligns with Senores' strategic focus on identifying and entering niche, under-penetrated generic formulations that present opportunities to serve unmet healthcare needs. This approach positions the company in specialized therapeutic areas with reduced competitive pressure.

Company Portfolio and Manufacturing Capabilities

Senores Pharmaceuticals operates as a global, research-driven pharmaceutical company with extensive manufacturing and development capabilities. The company's current portfolio encompasses significant regulatory approvals and pipeline products across multiple markets.

Portfolio Component Details
ANDA Portfolio 46 ANDAs with 133 strengths
Pipeline 22 ANDAs with 52 strengths in development
CMO/CDMO Operations 8 ANDAs and 24 products permitted for US distribution
CMO Pipeline 16 ANDAs and 57 strengths under development
Global Reach Over 394 product registrations across 40+ countries

Manufacturing Infrastructure

The company maintains a robust manufacturing infrastructure with facilities strategically located to serve both regulated and emerging markets. Senores operates two formulation manufacturing facilities - one USFDA-approved facility in Atlanta, US, which is DEA and TAABAA compliant for controlled substances, and another WHO-GMP approved facility in Chhatral, Ahmedabad, India.

Facility Type Location Regulatory Status
Formulations (US) Atlanta, USA USFDA, DEA, TAABAA approved
Formulations (India) Chhatral, Ahmedabad WHO-GMP approved
API Manufacturing Chhatral & Naroda, India Multiple country approvals
R&D Centers 1 in USA, 2 in India Advanced capabilities

The company also operates two API manufacturing facilities in India, located in Chhatral and Naroda near Ahmedabad, with regulatory approvals from over 10 countries. Additionally, Senores maintains strong research and development capabilities across three R&D sites to drive its differentiated product portfolio development.

Historical Stock Returns for Senores Pharmaceuticals

1 Day5 Days1 Month6 Months1 Year5 Years
+3.71%+8.32%+3.44%+46.27%+46.35%+46.35%
Senores Pharmaceuticals
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