Sep 2026 · PPT
Source: Bse
Pharma stocks · Micro cap · NSE
Aarti Pharmalabs (APL) is a globally recognized manufacturer of generic API, Xanthine derivatives, and a leading CDMO/CMO player in India. Part of the Aarti group, it operates 7 manufacturing units (3 USFDA approved), 3 R&D facilities, holds 63 patents, and 60 US DMFs. It commands 15-20% global market share in Xanthine derivatives.
SMA20 +8.2% / mo · MACD − · sector +4.9pp vs Nifty 500 (3M)
Latest mapped FPI equity flow was not positive. View sector evidence
Adjusted completed-session prices, rebased to 100
Weak fundamentals, while price trend supports entry. This looks more like momentum/speculation than a clean fundamental investment setup.
Weak U-Score but strong trend: momentum may be ahead of fundamentals.
Fundamental lens: valuation, quality, growth, balance sheet, and cash flow.
Revenue +38.9% · PAT +52.0% 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 +39% YoY · PAT +52% YoY · margin expansion · operating leverage
| Metric | This quarter | YoY | QoQ |
|---|---|---|---|
| Revenue | ₹536 Cr | +38.9% | -8.1% |
| EBITDA | ₹136 Cr | +46.2% | +20.4% |
| Operating margin | 25.0% | +100 bps | +600 bps |
| PAT | ₹76 Cr | +52.0% | +24.6% |
| PAT margin | 14.2% | +123 bps | +372 bps |
NDF means not disclosed in the current structured filing feed. It is intentionally not treated as zero.
Updated 21/10/2026
Trend interpretation, Stage 2, relative strength, volume and indicator evidence
Signals are conflicting — long-term uptrend intact. RSI 44. Wait for confirmation.
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 32 · legacy U-Score band WATCHLIST · 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: +1 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
Q4 FY26 consolidated revenue grew 3.3% YoY and 34.8% QoQ to INR 5,826 Mn, driven by record CDMO sales. However, consolidated EBITDA declined 10.6% YoY to INR 1,301 Mn, with margins contracting 349 bps YoY to 22.33%. FY26 standalone revenue grew 1.5% YoY, but EBITDA fell 4.8% to INR 4,061 Mn.
While Q4 FY26 showed strong sequential revenue growth, particularly in CDMO, and resolution of operational issues at Atali, the significant YoY decline in EBITDA and PAT margins for both the quarter and full year FY26 is concerning. Headwinds from input costs and limited pass-through ability, coupled with higher finance costs and depreciation, are impacting profitability despite revenue growth.
Latest issuer-disclosed distribution across 3 reported categories.
The CDMO/CMO segment logged its highest ever quarterly revenue at INR 155 Cr in Q4 FY26, and the company is expanding its on-ground sales presence to USA and EU.
Capacity expansion is ongoing to increase total Xanthine capacity to 9,000+ MTPA, targeting a global market share of 20-25% from the current 15-20%.
Phase 1 at the Atali greenfield site, with 450+ kL reactor capacity, is expected to be fully operational by June 2026, serving as a growth engine for CDMO/CMO.
The company is initiating R&D investment in FY27 towards TIDES (Peptides & Oligonucleotides) to expand its portfolio capabilities.
Capacity expansion is underway to increase total Xanthine capacity from the current 6,000 MTPA to 9,000+ MTPA. Commissioning is expected by June 2026.
Phase 1 at the Atali greenfield site, with 450+ kL reactor capacity, was ~80% operational by Q4 FY26 and is expected to be fully operational by June 2026.
The company is a non-Chinese dependent and fully backward integrated manufacturer of Xanthine derivatives, offering strong geographical diversification amidst the 'China+1' shift.
Beverage sales for Xanthine derivatives are predominantly driven by long-standing client relationships, ensuring a consistent revenue stream.
Ongoing geopolitical tensions have resulted in input and logistics price hikes.
Cost pass-through to customers is difficult in the API/Intermediates segments.
Recognition of fair value movement on a long-dated USD forward contract under FVTPL impacted reported profitability.
Ongoing geopolitical tensions are causing input and logistics price hikes, and the company faces difficulty in passing these costs through to customers in API/Intermediates.
Fair value movements on USD forward contracts have impacted reported profitability, indicating exposure to foreign exchange fluctuations.
Successful commissioning and ramp-up of Xanthine capacity to 9,000+ MTPA and full operationalization of Atali Phase 1 are critical for future growth targets.
Issuer guidance and extracted claims are tracked against later reported outcomes. Treat these as management statements, not IndiaPulse forecasts.
QoQ comparison is relevant for Q4 FY26 to assess sequential momentum in CDMO and the resolution of operational challenges at the Atali plant. YoY comparison is useful for evaluating overall business performance and margin trends, especially for standalone figures, as annual consolidated figures are explicitly stated as not comparable YoY due to a JV accounting change.
International sales constituted 54% of total geographical sales in FY26. Xanthine derivatives had 57% international sales, and API & Intermediates had 56% international sales in FY26.
The company has 11 new APIs under development (R&D/validation stage) and is working on 54 active CDMO projects, with 19 of these under different stages of development.
Aarti Pharmalabs holds 60 US DMF approvals and 44 CEP approvals. Its Dombivli Unit secured USFDA approval in 2023.
CDMO/CMO contributed 29.1%, API & Intermediates 28.3%, and Xanthine derivatives 42.6% to Q4 FY26 revenue.
FY27 capital expenditure is expected to be at similar levels to FY26, which reached approximately INR 400 Cr.
Management is targeting 15-18% revenue and EBITDA CAGR over the next 3-4 years on a standalone basis.
The company is evaluating a dedicated block for a specific CDMO project at Atali, with groundbreaking planned in FY27 and a 1-year completion target.
| Checkpoint | Current evidence | What to verify next |
|---|---|---|
| Xanthine Capacity Utilization | Currently operating at 6,000 MTPA. | Successful commissioning and ramp-up to 9,000+ MTPA post June 2026, and its impact on market share. |
| Atali Phase 1 Operational Status | ~80% operational by Q4 FY26, fully operational expected by June 2026. | Full operationalization, successful customer audits, and contribution to CDMO segment growth. |
| API/Intermediates Margin Trend | Under pressure from input costs with difficult cost pass-through. | Stabilization or improvement in margins, indicating better cost management or pricing power. |
| CDMO Project Conversion | 19 projects under development out of 54 active projects. | Conversion of development projects to commercial stage and addition of new customers/projects. |
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 32nd percentile of the scored universe and 22nd percentile within Pharma. Main check: results consistency is weak at 27/100.
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: 22nd pctile, median 70 · Micro: 17th pctile, median 73
63 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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