Jubilant Pharmova Limited (JUBLPHARMA.NS) Bundle
Dive into Jubilant Pharmova's latest financial picture where quarterly revenue climbed to ₹1,915.80 crore in Q4 FY25 (up 9.7% year‑on‑year) and full‑year sales reached ₹7,192.10 crore (an 8.24% increase), with the radiopharma division alone contributing nearly 46% of revenue in Q3 FY25 and a U.S. network of 52 radiopharmacies underpinning geographic expansion; profitability metrics show a sharp turnaround-Q4 net profit of ₹153.60 crore versus a prior‑year loss and FY25 net profit of ₹839.40 crore (up 988.72%), EPS at ₹53.13, EBITDA at ₹1,230 crore (up 24%) with a 220 bps margin expansion-balance‑sheet moves include a net debt/EBITDA improvement to 1.1x following a voluntary prepayment of USD 125 million, working capital days cut to 30.2, a proposed final dividend of ₹5 per share, and valuation metrics showing a P/E of 21.38x (about a 44% discount to peers) and P/B of 2.87x (about a 21% discount), all of which set the stage for a deeper look at risks, liquidity, and growth opportunities in the sections that follow-read on to unpack what these figures mean for investors.
Jubilant Pharmova Limited (JUBLPHARMA.NS) - Revenue Analysis
Jubilant Pharmova reported steady top-line expansion across quarterly and annual periods, driven largely by radiopharmaceuticals while contract manufacturing and generics contributed incremental gains. Key headline figures and segment/geography details are summarized below.
| Period | Revenue (₹ crore) | YoY Growth |
|---|---|---|
| Q4 FY25 | 1,915.80 | +9.7% vs Q4 FY24 (1,746.40) |
| Full Year FY25 | 7,192.10 | +8.24% vs FY24 (6,644.80) |
- Quarterly momentum: Q4 FY25 revenue of ₹1,915.80 crore, up 9.7% year-on-year from ₹1,746.40 crore in Q4 FY24.
- Annual performance: FY25 consolidated revenue of ₹7,192.10 crore, an 8.24% increase from FY24's ₹6,644.80 crore.
Segment-level contributions and trends:
- Radiopharmaceuticals: Nearly 46% of total revenue in Q3 FY25; recorded ~12% growth in Q3 FY25, remaining the primary growth engine.
- Contract Manufacturing: Modest sequential and YoY increases driven by new commercial supply agreements and capacity utilization improvements.
- Generics: Incremental growth supported by product launches and stable demand in key markets.
| Segment | Notable Data / Impact |
|---|---|
| Radiopharma | ~46% of revenue (Q3 FY25); ~12% growth in Q3 FY25; network of 52 radiopharmacies in the U.S. |
| Contract Manufacturing | Small but steady growth; contribution aided by commercial scale-up and customer wins. |
| Generics | Moderate growth; new launches contributing to breadth of offering. |
- Geographical expansion: Operates 52 radiopharmacies across the United States, reinforcing recurring revenue potential and market reach.
- Product diversification: Launched Technetium (Tc 99m) Sulfur Colloid Injection in Q3 FY24, part of a broader strategy to expand radiopharma product portfolio.
For broader corporate context and history, see: Jubilant Pharmova Limited: History, Ownership, Mission, How It Works & Makes Money
Jubilant Pharmova Limited (JUBLPHARMA.NS) - Profitability Metrics
Jubilant Pharmova delivered a decisive profitability turnaround in FY25, driven by stronger operating performance across its business units, margin recovery and one-time adjustments reflected in normalized results.
- Quarterly net profit (Q4 FY25): ₹153.60 crore vs. net loss of ₹58.60 crore in Q4 FY24.
- Annual net profit (FY25): ₹839.40 crore, up 988.72% from ₹77.10 crore in FY24.
- Earnings per share (EPS): ₹53.13 in March 2025 vs. negative ₹3.83 in March 2023.
- EBITDA (FY25): ₹1,230 crore, growth of 24% year-over-year.
- EBITDA margin: expanded by 220 basis points in FY25.
- Normalized PAT (FY25): ₹415 crore, up 112% after adjusting for exceptional items and tax.
| Metric | Period | Value (₹ crore) | YoY Change | Notes |
|---|---|---|---|---|
| Net Profit (Quarterly) | Q4 FY25 | 153.60 | - (Turnaround from loss) | Recovered from Q4 FY24 loss of ₹58.60 crore |
| Net Profit (Annual) | FY25 | 839.40 | +988.72% | Versus ₹77.10 crore in FY24 |
| EPS | Mar 2025 | 53.13 (₹) | Improved from -3.83 (Mar 2023) | Reflects substantial earnings recovery |
| EBITDA | FY25 | 1,230.00 | +24% | Driven by strong operations across units |
| EBITDA Margin | FY25 | Expanded by 220 bps | Improved efficiency | Margin expansion contributed to earnings leverage |
| Normalized PAT | FY25 | 415.00 | +112% | After adjusting for exceptional items & tax |
Key drivers behind these metrics include improved utilization, cost controls and favorable product mix across pharmaceuticals and life‑science services. For strategic context, see: Mission Statement, Vision, & Core Values (2026) of Jubilant Pharmova Limited.
Jubilant Pharmova Limited (JUBLPHARMA.NS) - Debt vs. Equity Structure
Key financial shifts in FY25 reflect a deliberate move toward deleveraging and maintaining equity stability.
- Net Debt to EBITDA improved from 2.5x (Mar 2024) to 1.1x (Mar 2025) after a voluntary prepayment of USD 125 million in FY25.
- Voluntary debt prepayment: USD 125 million executed in FY25 as a primary driver of leverage reduction.
- Promoter holding remained stable at 50.68% as of March 2025, indicating consistent equity backing.
- Interest coverage: materially strengthened in FY25 driven by higher net profit, though precise coverage ratios are not disclosed.
- Debt composition (short-term vs. long-term): specifics not provided in available disclosures.
- Equity capital: no significant changes reported in recent periods.
| Metric | Mar 2024 | Mar 2025 | Notes |
|---|---|---|---|
| Net Debt to EBITDA | 2.5x | 1.1x | Improvement driven by USD 125M prepayment |
| Debt Reduction (FY25) | USD 125 million prepayment | Voluntary prepayment reported | |
| Promoter Holding | - | 50.68% | Stable promoter stake as of Mar 2025 |
| Interest Coverage | Not disclosed | Not disclosed | Improved ability to cover interest implied by higher net profit |
| Debt Composition | Not specified | Short-term vs. long-term split not available | |
| Equity Capital Changes | No significant changes | Equity base remains stable | |
- Implications for investors:
- Lower leverage (1.1x) reduces refinancing and solvency risk.
- Stable promoter holding supports continuity in strategic direction.
- Absent debt composition detail increases the importance of monitoring maturity profiles in future disclosures.
- Actionable monitoring points:
- Track quarterly debt levels and any further prepayments or refinancings.
- Watch for explicit interest coverage ratios in upcoming filings.
- Monitor disclosures for short-term vs. long-term debt breakdown and any equity issuance.
Related reference: Mission Statement, Vision, & Core Values (2026) of Jubilant Pharmova Limited.
Jubilant Pharmova Limited (JUBLPHARMA.NS) - Liquidity and Solvency
Jubilant Pharmova's recent disclosures point to an improving short-term liquidity profile and sustained operational cash generation, while some standard ratio metrics remain undisclosed in public releases.
- Current Ratio: Specific current ratio figures are not provided in the available sources.
- Quick Ratio: Quick ratio details are not available in the provided information.
- Cash Flow from Operations: The company has reported strong cash flow from operations, supporting its liquidity position (exact figure not disclosed in the referenced summary).
- Working Capital Management: Working capital requirement reduced from 59.9 days to 30.2 days, indicating improved efficiency in receivables/inventory/payables management.
- Solvency Ratio: Specific solvency ratios are not detailed in the available sources.
- Dividend Distribution: The board has proposed a final dividend of ₹5 per equity share for FY25, reflecting confidence in cash generation and balance sheet strength.
| Metric | Latest Reported Value / Note |
|---|---|
| Current Ratio | Not provided |
| Quick Ratio | Not provided |
| Cash Flow from Operations | Reported as strong (exact amount not disclosed in summary) |
| Working Capital (Days) | Reduced from 59.9 days to 30.2 days |
| Solvency Ratio | Not provided |
| Dividend (Final, FY25) | ₹5 per equity share (board proposal) |
For further context on shareholding, investor activity and rationale that may influence liquidity perceptions, see: Exploring Jubilant Pharmova Limited Investor Profile: Who's Buying and Why?
Jubilant Pharmova Limited (JUBLPHARMA.NS) - Valuation Analysis
- P/E Ratio (as of 19 Jun 2025): 21.38× - trading at a 44% discount to peers' median of 38.24×.
- P/B Ratio: 2.87× - ~21% below peers' median of 3.63×.
- Earnings Momentum: Net profit growth for FY25 of 988.72% (year-over-year).
- Dividend: Proposed dividend of ₹5.00 per share for FY25 (yield % not specified in available sources).
- Market Cap / EV: Specific market capitalization and enterprise value figures not available in provided sources.
| Metric | Value | Peer Median / Note |
|---|---|---|
| Price-to-Earnings (P/E) | 21.38× (19‑Jun‑2025) | Peer median 38.24× (JUBLPHARMA at -44%) |
| Price-to-Book (P/B) | 2.87× | Peer median 3.63× (JUBLPHARMA at -21%) |
| Net Profit Growth (FY25) | +988.72% | Significant outperformance year-over-year |
| Proposed Dividend (FY25) | ₹5.00 per share | Dividend yield % not specified |
| Market Capitalization | Not provided | - |
| Enterprise Value (EV) | Not provided | - |
- Interpretation cues for investors:
- The P/E and P/B discounts versus peers imply relative valuation support if earnings sustainability holds.
- Extraordinary FY25 profit jump (988.72%) requires scrutiny of drivers-one-off items, operational improvement, or accounting effects.
- Dividend proposal (₹5) adds income component, but yield must be computed against current share price before relying on cash return assumptions.
Jubilant Pharmova Limited (JUBLPHARMA.NS) - Risk Factors
Jubilant Pharmova operates across contract manufacturing, radiopharma, specialty pharma and life-science ingredients. Investors should weigh several company-specific and industry-wide risks that can materially affect cash flows, margins and valuation.- Regulatory Compliance - Frequent inspections and approvals: Jubilant Pharmova's manufacturing and radiopharmaceutical facilities are subject to multiple regulators (DCGI, US FDA, EMA, etc.). Non-compliance can lead to plant shutdowns, warning letters or product recalls, directly impacting revenue. Historically, regulatory actions in the pharma sector have caused quarter-over-quarter revenue swings of 10-30% for impacted product lines.
- Currency Fluctuations - Revenue mix exposure: A material portion of revenues is exported (API, CDMO and radiopharma exports). FX volatility (INR vs USD/EUR) can swing reported topline and margins; a 5% rupee appreciation can erode EBITDA by several percentage points for export-heavy quarters.
- Competitive Landscape - Pricing pressure and margin erosion: The company competes with global generics, CDMOs and niche radiopharma players. Increased competition can compress prices; in commoditised API segments, price declines of 10-25% over 12-24 months are common.
- Supply Chain Disruptions - Raw-material and logistics risk: Reliance on specific chemical intermediates and radiomaterials exposes operations to supply shocks. Disruptions (e.g., logistic bottlenecks, single-source suppliers) can increase input costs by 8-20% in affected periods.
- Intellectual Property Risks - Patent cliffs and generic entry: For specialty molecules and formulations, patent expiries can invite rapid generic entry; typical revenue declines post-patent expiry range from 40% to >80% for the affected SKU over 1-3 years.
- Operational Risks - Scaling and integration: Expansion of manufacturing capacity or new facility commissioning carries execution risk (cost overruns, delayed regulatory approvals). Capital projects in pharma frequently exceed budgets by 10-30%, pressuring near-term ROCE.
| Metric | Value (most recent reported) | Notes / Sensitivity |
|---|---|---|
| Revenue | ₹5,531 crore | Mix across CDMO, Radiopharma, APIs and formulations - exports significant |
| EBITDA Margin | ~16% | Subject to product mix and regulatory-related downtime |
| Net Profit | ₹312 crore | Volatile due to one-offs, forex and exceptional items |
| Net Debt | ₹1,200 crore | Leverage sensitive to capex for capacity expansion |
| R&D / Tech Spend | ~₹150-220 crore | Investment in radiopharma and specialty molecules; supports long-term pipeline |
- Regulatory event scenario - a major inspection failure at a key plant can reduce revenue from that plant by 50-100% until remediation; associated remediation capex and lost sales can cut annual EBITDA by several hundred crores depending on the plant size.
- FX shock scenario - a sustained 10% INR appreciation versus USD/EUR could reduce reported revenues and EBITDA margins materially; hedging programs and natural FX offsets in costs moderate but do not eliminate exposure.
- Supply-chain shock scenario - raw-material price spikes or single-source supplier failure can increase COGS by mid-to-high single digits to low double digits, compressing margins and pressuring working capital.
- Regulatory inspection history and remediation timelines for major plants.
- Currency hedging policies and the share of revenues invoiced in foreign currency.
- Order book and backlog in CDMO and radiopharma segments (visibility into contracted revenues).
- Capex plans, expected commissioning dates, and projected incremental EBITDA contribution.
- Patent status and exclusivity timelines for specialty products; pipeline timelines for new formulations.
Jubilant Pharmova Limited (JUBLPHARMA.NS) - Growth Opportunities
Jubilant Pharmova's strategic thrust centers on radiopharmaceuticals, geographic scale-up, product diversification and balance-sheet optimization. The company's near- to medium-term moves create multiple levers for revenue and margin expansion while unlocking shareholder value via non-core stake monetizations.- Radiopharmaceutical Expansion: Planned launches in the radiopharma category (including diagnostic and therapeutic tracers) are positioned to leverage growing global demand for molecular imaging and theranostics.
- Geographical Diversification: Scaling the U.S. radiopharmacy network and expanding into other regions (Europe, select APAC markets) aims to capture higher-margin per-dose economics and reduce concentration risk.
- Product Portfolio Diversification: Introduction of Technetium (Tc 99m) Sulfur Colloid Injection and other Tc-99m kits broadens recurring consumable revenues tied to imaging procedures.
- Strategic Investments: The sale of a 25.8% stake in Sofie Biosciences Inc. provides liquidity for core expansion and deleveraging while signaling portfolio pruning to focus on radiopharma and CDMO strengths.
- Operational Efficiency: Working capital improvements, tighter inventory turns and selective debt reduction can materially improve free cash flow and financial flexibility.
- Regulatory Approvals: Timely approvals (FDA/EMA/other national agencies) for new radiopharmaceuticals and sterile products can accelerate payback and open new reimbursement-backed revenue streams.
| Growth Vector | Key Action | Near-term Impact (Est.) | Medium-term Impact (Est.) |
|---|---|---|---|
| Radiopharma Product Launches | Introduce Tc-99m Sulfur Colloid & additional kits | Incremental revenue: ₹80-150 crore p.a. | Revenue CAGR uplift: +8-12% for radiopharma business |
| U.S. Radiopharmacy Expansion | Increase network density and distribution | Improve per-dose margins by 3-6% | Market share rise from single-digit to mid-teens % in target regions |
| Stake Sale (Sofie Biosciences) | Monetized 25.8% stake | One-time cash inflow (reported): ~USD 53 million (~₹430 crore) | Redeploy to capex, debt reduction or radiopharma R&D |
| Working Capital & Debt | Improve DSO/Inventory days; repay high-cost debt | FCF improvement: ₹50-120 crore p.a. | Net debt/EBITDA reduction by 0.5-1.0x over 12-24 months |
| Regulatory Approvals | FDA/EMA/Local registrations for new products | Access to reimbursed markets; initial contract wins | Sustained revenue base for licensed products; margin accretion |
- Commercial ramp assumptions: Early-stage radiopharmaceutical launches typically show low initial volumes with steep volume growth in years 2-4-model scenarios should assume 25-40% year-over-year unit growth after market entry.
- Margin sensitivity: Radiopharma products and radiopharmacies usually deliver higher gross margins versus legacy sterile generics; a successful U.S. expansion can lift consolidated gross margin by 200-400 bps over time.
- Capital allocation priorities: Proceeds from strategic disposals (e.g., Sofie stake sale) can be allocated across (a) capex for radiopharma capacity, (b) targeted M&A to accelerate U.S. footprint, and (c) debt reduction to lower interest burden.

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