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₹1,273Cr
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SHUKRAPHAR
VS
| Quarter | Sep 2025 |
|---|
|
Growth YoY Revenue Growth YoY% | | | 269.9 |
| 7 | 6 | 12 |
Operating Profit Operating ProfitCr |
| 37.2 | -7.1 | 69.3 |
Other Income Other IncomeCr | 1 | 2 | 1 |
Interest Expense Interest ExpenseCr | 0 | 0 | 0 |
Depreciation DepreciationCr | 1 | 1 | 1 |
| 4 | 0 | 27 |
| 1 | -2 | 6 |
|
Growth YoY PAT Growth YoY% | | | 544.3 |
| 29.9 | 40.5 | 52.0 |
| 0.1 | 0.1 | 0.5 |
| Financial Year | Mar 2025 |
|---|
|
| |
| 20 |
Operating Profit Operating ProfitCr |
| 39.1 |
Other Income Other IncomeCr | 4 |
Interest Expense Interest ExpenseCr | 1 |
Depreciation DepreciationCr | 3 |
| 13 |
| 4 |
|
| |
| 29.4 |
| 0.2 |
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| Financial Year | Mar 2025 |
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Profitability Ratios Profitability Ratios |
| 75.1 |
| 39.1 |
| 29.4 |
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### **Overview**
Shukra Pharmaceuticals Limited is a publicly listed Indian pharmaceutical company headquartered in Ahmedabad, Gujarat. The company specializes in the development, manufacturing, and export of high-quality pharmaceutical formulations for both domestic and international markets. With a strong foundation in regulatory compliance, R&D, and scalable manufacturing, Shukra is strategically positioning itself for diversified growth in generics, biosimilars, specialty drugs, and medical devices.
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### **Core Business and Operations**
- **Segments**: The company operates primarily in the **pharmaceutical segment**, with a nascent laboratory services segment that has not yet commenced meaningful commercial activity.
- **Manufacturing**: Shukra operates a **10-acre WHO-GMP and FDA-approved manufacturing facility** in Rakanpur, Gandhinagar, equipped for solid oral dosage forms (tablets, capsules) and small-volume parenteral injections (vials and ampoules).
- **Product Portfolio**: Broad therapeutic coverage including:
- Antibiotics (penicillin, cephalosporin)
- Antivirals, antifungals, anti-tuberculosis drugs
- Analgesics, corticosteroids, vitamins, beta blockers
- Anti-depressants, anti-malarials, diuretics, anti-ulcer agents
- **Manufacturing Strength**: Emphasis on **in-house production of critical and precision components** to ensure quality control, supply chain reliability, and regulatory adherence.
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### **Market Presence and Export Strategy**
- **Geographic Reach**: Direct presence in **Australia, Kenya, Uganda, the UK, Sri Lanka, Mauritius, Yemen, Cambodia, Myanmar, Vietnam, Peru, and Guatemala**. Indirect reach via export partners into Africa, Europe, the Americas, the Middle East, and the Pacific Islands.
- **Export Model**: Relies on a network of **international merchant exporters** based in the **U.K., Denmark, Australia, and Singapore** who distribute products to secondary markets, including NGOs, military organizations, and government health systems.
- **Regulatory Approvals**: Products and facilities are approved by health ministries in **Nigeria, Ghana, Sierra Leone, Kenya, Uganda, Congo, Yemen, Cambodia, and others**. Holds WHO-GMP certification since **1998** and multiple country-specific GMP certifications.
- **Strategic Expansion**: Actively targeting **underpenetrated markets** in **Japan, China, Indonesia, Latin America, and East Asia**, with focus on navigating complex regulatory landscapes and forming localized distribution partnerships.
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### **Recent Strategic Developments (2023–2025)**
#### **Expansion & Infrastructure (2025)**
- **Branch Offices (Jul 2025)**: Opened four new branches in **Mumbai, Gurgaon (NCR), Bangalore, and Kolkata** to enhance access to institutional clients, government tenders, and high-growth domestic markets.
- **Distributorship Agreements (Sep 2025)**:
- Secured distributorship rights for **medical devices and surgical instruments** from leading global manufacturers.
- Partners include **Trivitron (hematology analyzers), Nidek (eye care), Oculus (tonometers), Resono (dry eye systems), DJO Global (shockwave therapy), Remescan (X-ray), and Convatec (wound dressings)**.
- Partnership with **Wockhardt Limited** to expand access to Indian government and institutional healthcare networks.
#### **Strategic Alliances & Diversification (Oct–Sep 2025)**
- Forming **strategic alliances** to enter the **medical devices and surgical instruments** market—diversifying revenue streams beyond pharmaceuticals.
- Exploring **technology collaborations** to enter the **biosimilars and specialty drug** segments by 2026–2030, aligning with global trends in advanced therapeutics.
- The **global biosimilars market** is projected to exceed **USD 60 billion by 2030**, presenting a significant growth opportunity.
#### **New Ventures (Aug 2023)**
- Launched **Shukra Wellness**, a subsidiary focused on marketing **Mouth Dissolving Strips (MDS)** for prescription and nutraceutical products.
- Partnered with a third-party manufacturer to target niche markets in **Brazil, Russia, Latin America, Africa, and Asia**.
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### **Growth Strategy and Competitive Advantages**
- **Differentiation Drivers**:
- Strong **R&D capabilities** and focus on developing patentable platform technologies.
- **WHO-GMP certified since 1998**—a key trust signal for global buyers.
- **Multi-country product registrations** creating a competitive moat and enabling a "one-stop-shop" for international clients.
- B2B model with focus on contract manufacturing and technical partnerships with global pharma firms.
- **Scalability**: Proven ability to scale—business volume **tripled in FY 2022–23**; revenue grew **2.95x between FY 2022 and FY 2024**.
- **Certifications & Compliance**:
- Pursuing **ISO 9000 certification** to strengthen quality infrastructure.
- Member of **Pharmexcil** (Pharmaceutical Export Promotion Council of India).
- **High Switching Costs**: Due to the time-intensive nature of regulatory registrations, customers are less likely to switch suppliers.
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### **Challenges and Risks**
- **Supply Chain Vulnerability**:
- No long-term agreements with **raw material (API) suppliers**, exposing the company to price volatility and supply disruptions (e.g., during pandemics or geopolitical events).
- **Customer Concentration Risk**:
- No long-term contracts with customers; revenue depends on dynamic demand and relationships.
- **Regulatory Hurdles in New Markets**:
- Expansion into **Japan, China, and Latin America** requires navigating stringent regulatory standards, localization, and infrastructure readiness.
- **Operational Constraints in Advanced Therapeutics**:
- While India has early experience in biosimilars (e.g., Reditux), scaling biologics faces challenges in infrastructure and regulatory alignment—posing both opportunity and risk.
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### **Leadership and Governance**
- **Promoter-Technocrat Leadership**: Led by industry-experienced promoters with hands-on expertise in pharmaceutical manufacturing and global compliance.
- **Commitment to Quality**: Uninterrupted adherence to **WHO-GMP standards since 1998**, reflecting a culture of quality and continuous improvement.