Announcement under Regulation 30 (LODR)-Press Release / Media Release 8 Oct - Lupin received US FDA approval for Phytonadione Injectable Emulsion USP; estimated U.S. sales $52.3 million.
Source: Bse
Pharma stocks · Mid cap · NSE
Lupin Limited is a global pharmaceutical company with operations in over 100 countries. It focuses on generics, complex generics, biosimilars, and specialty products, supported by a strong R&D and manufacturing footprint. The company aims to deliver treatments across various therapeutic areas.
full bear SMA stack · SMA20 -5.1% / mo · MACD + · near 52W low · sector +4.3pp vs Nifty 500 (3M)
FPI equity flow was positive in both fortnights, but the sector index is below its 100-session average. View sector evidence
Today's candle is provisional from the latest intraday quote; completed-candle scans remain unchanged.
Adjusted completed-session prices, rebased to 100
Strong fundamentals, management evidence is still limited to a financial-only Trust Lite signal, price trend is neutral, and recent execution is consistent.
Fundamental lens: valuation, quality, growth, balance sheet, and cash flow.
Revenue +32.0% · PAT +16.1% YoY
Price trend and sector-relative-strength timing.
Legacy margin-of-safety estimate; the revised evidence label remains in shadow validation.
Financial-only signal; management claim evidence is not sufficient yet.
Fundamentals, quarterly history, margins, returns and balance-sheet evidence
Rev +32% YoY · PAT +16% YoY · margin expansion · +11% QoQ
| Metric | This quarter | YoY | QoQ |
|---|---|---|---|
| Revenue | ₹8,277 Cr | +32.0% | +10.7% |
| EBITDA | ₹2,450 Cr | +41.9% | -1.4% |
| Operating margin | 30.0% | +200 bps | -300 bps |
| PAT | ₹1,417 Cr | +16.1% | -3.5% |
| PAT margin | 17.1% | -236 bps | -253 bps |
NDF means not disclosed in the current structured filing feed. It is intentionally not treated as zero.
Updated 20/10/2026
Trend interpretation, Stage 2, relative strength, volume and indicator evidence
Trend is weak — long-term trend down. RSI 32.
Mechanical read from the price + indicator series above. Not a recommendation — technical setups can reverse without warning, especially around earnings and macro events.
U-Score 83 · legacy U-Score band DEEP VALUE · valuation evidence and comparable companies
Top U-Score contributors and drags from the latest stored fundamentals.
Healthcare valuation needs both earnings quality and regulatory/pipeline context.
This shows the stored score trend when snapshots exist, and also compares the latest stored nightly score with a live recompute from current fundamentals and price.
12 stored score snapshots. Latest stored move: +0 points.
Business-comparable peers in Pharma — ranked by industry, sub-sector, theme-tag overlap, market cap, and U-Score similarity. Green cells mark the best available peer metric in this table.
Growth engines, risks, management commitments and evidence-backed delivery
Lupin reports strong Q4 FY26 sales growth of 33% YoY, driven by North America and LATAM, with PAT up 89% YoY. EBITDA margin expanded significantly YoY but saw a slight QoQ dip.
Lupin's Q4 FY26 performance shows robust growth, particularly in North America due to new product launches, and continued outperformance in the India market. While profitability improved significantly YoY, a slight sequential moderation in EBITDA margin and ongoing compliance remediation at some sites warrant monitoring.
Latest issuer-disclosed distribution across 5 reported categories.
Growth in the US market is driven by new product launches, with 15 products launched in FY26 and a plan to launch 100+ NPLs by FY31.
Strong pipeline of 45+ Injectables and 20+ inhalation products, with a target to launch 5+ biosimilars by FY31.
India business focuses on maximizing chronic share to ~70% by FY31, with key segments like Cardiology and Respiratory outperforming the market.
Company plans to target alliances/M&A for mid-size companies, brands & portfolios, and in-license new products via partnerships including GLP-1s.
Completed expansion of Dabhasa manufacturing facility to scale peptide platform and enhance CRDMO capabilities at Lupin Manufacturing Solutions.
Aurangabad received ANVISA & CDSCO approval, Pune Biotech received CDSCO approval, Nagpur Unit 1 received WHO and Ukraine approval.
Received European Commission Approval for Biosimilar Ranibizumab (RanluspecTM), strengthening specialty pharma footprint in Europe.
Filed 10+ ANDAs in FY26, including two 505(b)(2)s, and plans to file 15+ in FY27, indicating future launch potential.
Growth in US was offset by additional generic competition in base business and lower seasonal product sales, leading to mid-single digit price decline.
Anti-diabetes segment in India was impacted by LOE in the in-licensed portfolio, growing 9.4% vs IPM growth of 12.2% in FY26.
Pithampur Unit II has an OAI status, and remediation is in progress. Tarapur and Mandideep Unit-1 are also identified as remediation sites.
Additional generic competition in the US base business and price declines in key products like Albuterol pose ongoing challenges.
Issuer guidance and extracted claims are tracked against later reported outcomes. Treat these as management statements, not IndiaPulse forecasts.
YoY comparison is crucial for assessing overall growth and margin expansion against the previous year. QoQ comparison provides insight into sequential momentum, recent market dynamics, and profitability trends.
India Rx business grew by 14.5% YoY in Q4 FY26, outperforming IPM growth of ~9.9% in FY26.
North America sales were 35,145 mn INR, growing 55% YoY and 6% QoQ in Q4 FY26, driven by new product launches.
Launched Dapagliflozin Tabs (gFarxiga®) and Sugammadex Inj (gBridion®) in the US during Q4 FY26.
Goa facility received EIR (VAI). Responses submitted for Ankleshwar & Somerset (PAI). Pithampur Unit II (OAI) response submitted, remediation in progress.
Management targets all sites to have satisfactory compliance status, with successful FDA inspections for several units in the last 12 months.
Management plans to launch 20+ products in India in FY27, following healthy launches across therapies in FY26.
Management plans to file 15+ ANDAs in FY27, building on 10+ ANDAs filed in FY26.
| Checkpoint | Current evidence | What to verify next |
|---|---|---|
| Pithampur Unit II US FDA Status | OAI, response submitted, remediation in progress. | Resolution of OAI status and receipt of EIR (VAI/NAI). |
| India Product Launches (FY27) | Plan to launch 20+ products. | Execution and market acceptance of new product launches in India. |
| US ANDA Filings (FY27) | Plan to file 15+ ANDAs. | Progress on ANDA filings and subsequent approvals for new products in the US market. |
Verification checkpoints are IndiaPulse research interpretation, not investment advice.
Trust asks: does management behaviour match later outcomes? Higher is better, but confidence and evidence depth matter as much as the number.
Limited evidence: Claim history is still being built. It ranks around the 98th percentile of the scored universe and 98th percentile within Pharma. No major sub-score weakness stands out.
This is a financial-behaviour screen, not a claim-tested management reliability verdict.
Financial behaviour is scored, but management claims do not yet have enough outcome checks.
overall median 67 · Pharma: 98th pctile, median 70 · Mid: 93rd pctile, median 76
183 documents have extracted text, but claim history is not strong enough yet.
0 claims extracted · No contradicted claim yet
Read Trust alongside U-Score, result consistency, and technical trend. A cheap stock with weak Trust needs a larger margin of safety; a high Trust score does not make an expensive stock attractive by itself.
Read low sub-scores as due-diligence warnings, not automatic sell signals.
Trust Lite uses financial behaviour only. Prefer claim-tested Trust when enough concall claims have later outcomes.
Latest exchange and company disclosures found within the past two years.
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