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Dr. Reddy's Laboratories Ltd. (IN:DRREDDY)
:DRREDDY
India Market

Dr. Reddy's Laboratories Ltd. (DRREDDY) AI Stock Analysis

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IN:DRREDDY

Dr. Reddy's Laboratories Ltd.

(DRREDDY)

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Outperform 70 (OpenAI - 5.2)
Rating:70Outperform
Price Target:
₹1,359.00
▲(6.14% Upside)
The score is driven primarily by strong profitability and a conservative balance sheet, tempered by weaker cash conversion. The earnings call was constructive on guidance and pipeline progress, but near-term headwinds (post-Lenalidomide margin pressure and U.S. regulatory uncertainty) keep the score from being higher, while technicals are mixed and valuation is only moderately supportive.
Positive Factors
High and sustainable margins
Consistently strong gross and net margins provide structural profitability advantages vs peers, enabling reinvestment in R&D, branded growth and capacity. High margins also create a buffer against pricing cycles, supporting durable cash generation and return metrics over the medium term.
Conservative balance sheet and liquidity
A net cash surplus and low leverage give management flexibility to fund capex, complete integrations, and sustain pipeline investments without immediate financing. This financial headroom lowers execution risk for launches and M&A, improving resilience to regulatory or market delays.
Diversified growth engines and pipeline momentum
Broad exposure across branded India, emerging markets, generics, APIs, biosimilars and CDMO plus tangible semaglutide and abatacept progress reduces reliance on any single product. Multiple secular growth drivers and an active filing pipeline support sustained revenue diversification and secular growth over 2–3 years.
Negative Factors
Weak cash conversion
Earnings are not translating into proportional cash, indicating working‑capital or investment drains. Persistently low cash conversion constrains internal funding for R&D, capex and acquisitions, increases reliance on external financing and magnifies execution risk during margin or revenue pressure.
Margin compression post-Lenalidomide
A step‑down in high‑margin product revenue and broader pricing pressure reduces structural profitability, limiting free cash generation and ROCE. If mix shifts toward lower‑margin unbranded generics persist, reinvestment capacity and long‑term returns could be permanently impaired.
Regulatory risk for key biologics and inspections
Regulatory setbacks and facility observations can materially delay high‑value biologic launches, compress projected revenue and ROI from biosimilars, and strain partner relationships. Prolonged re‑inspections or CRLs increase execution uncertainty for products that drive medium‑term growth.

Dr. Reddy's Laboratories Ltd. (DRREDDY) vs. iShares MSCI India ETF (INDA)

Dr. Reddy's Laboratories Ltd. Business Overview & Revenue Model

Company DescriptionDr. Reddy's Laboratories Ltd. (DRREDDY) is a global pharmaceutical company based in India, specializing in the development, manufacture, and marketing of a wide range of generic and branded medications. The company operates across various sectors, including pharmaceuticals, active pharmaceutical ingredients (APIs), and biotechnology. DRREDDY's core products include prescription medications across multiple therapeutic areas such as oncology, cardiology, and dermatology, as well as over-the-counter products and biosimilars.
How the Company Makes MoneyDr. Reddy's generates revenue primarily through the sale of generic pharmaceuticals, which constitute a significant portion of its earnings. The company develops and markets a diverse portfolio of generic drugs, often capitalizing on the expiration of patents for branded medications. In addition to generics, revenue is also derived from the sale of proprietary drugs and biosimilars. Dr. Reddy's has established partnerships with various healthcare organizations and distributors to enhance its market reach and expand its global footprint. The company's revenue is further supported by its focus on research and development, allowing it to innovate and introduce new products. Additionally, it derives income from the manufacturing of APIs for third-party clients, contributing to its overall financial performance.

Dr. Reddy's Laboratories Ltd. Earnings Call Summary

Earnings Call Date:Jan 21, 2026
(Q3-2026)
|
% Change Since: |
Next Earnings Date:May 08, 2026
Earnings Call Sentiment Neutral
The quarter shows resilience in core branded businesses (India, emerging markets, NRT) with meaningful product-launch and pipeline progress, healthy cash position and strategic collaborations. However, earnings and margins were pressured by lower Lenalidomide revenue, pricing erosion in unbranded generics, elevated SG&A and one-time labor provisions, and regulatory uncertainties for key biologics in the U.S. The business is executing on strategic priorities and long-term growth drivers, but near-term financial headwinds and regulatory timing create caution.
Q3-2026 Updates
Positive Updates
Consolidated Revenue Growth
Consolidated revenue of INR 8,727 crore (USD 971m) in Q3 FY'26, up 4.4% YoY (down 0.9% QoQ); underlying base business (ex-Lenalidomide) delivered double-digit growth aided by favorable forex.
Strong India and Emerging Markets Performance
India revenue INR 1,603 crore, up 19% YoY (2% QoQ); organic India growth ~17%–18% excluding recent Stugeron acquisition. Emerging markets revenue INR 1,896 crore, up 32% YoY and 15% QoQ; Russia grew ~21% YoY and 16% QoQ in constant currency.
Adjusted Profitability Metrics
Reported EBITDA INR 2,049 crore (USD 228m); reported EBITDA margin 23.5% (down YoY), adjusted EBITDA margin 24.8% excluding one-time labor-code provision (company cites ~25% underlying EBITDA margin).
Pipeline and Regulatory Progress — Semaglutide & Abatacept
Received semaglutide marketing authorization in India, COPP filings underway in emerging markets and Health Canada response submitted (goal date by May). BLA for IV abatacept filed in Dec 2025 on schedule; subcutaneous abatacept US filing planned July 2026.
Business Development Wins
Strategic collaboration with Immutep for Eftilagimod Alfa (USD 20m upfront, up to USD 350m in milestones + royalties); launched Hevaxin (Hepatitis-E vaccine) in India; continued integration of acquired NRT business (85% by value under operational control).
Product Launches and Filings Momentum
Launched multiple products: 6 new products in North America, 10 new generics across markets, 30 new products across emerging markets, 2 new brands in India. Filed 31 DMFs globally and completed 28 global generic filings in the quarter.
Regulatory Inspection Outcomes and CDMO Wins
USFDA inspection at API facility CTO-SEZ returned 0 observations; Aurigene (CDMO) was exclusive API manufacturer for 2 novel USFDA-approved drugs in 2025 and delivered AI-assisted discovery programs, supporting future CDMO revenue growth.
Strong Balance Sheet and Cash Generation
Net cash surplus of INR 3,069 crore (USD 342m) as of Dec 31, 2025. CapEx in Q3 INR 669 crore (USD 75m) and free cash flow INR 374 crore (USD 42m). Currency hedges in place (USD ~481m through Mar 2027).
Negative Updates
Lenalidomide Decline and North America Pressure
Lower Lenalidomide sales materially impacted U.S. results; North America generics revenue $338m, down 16% YoY and 9% QoQ, with the company noting the decline was primarily due to Lenalidomide and pricing pressure.
Margin Compression
Consolidated gross profit margin declined to 53.6%, down 505 basis points YoY and 104 bps QoQ. Reported EBITDA fell 11% YoY and 13% QoQ; PAT attributable to equity holders declined 14% YoY and 16% QoQ. Company warns global generics gross margin may normalize to 50%–55% post-Lenalidomide.
One-Time Labor-Code Provision Impact
One-time provision related to changes in implied benefit obligations under new Indian labor law codes (disclosed in Q&A as ~INR 117 crore) reduced reported EBITDA and pushed adjusted metrics higher after exclusion.
Regulatory Setbacks for Biologics in the U.S.
Denosumab BLA received a CRL tied to partner Alvotech's manufacturing inspection — approval timing uncertain (company expects potential delay into FY'27 or later). Rituximab received a post-application action letter related to Bachupally facility; reinspection and timeline remain uncertain (>6 months risk).
Form 483 Observations at a Manufacturing Site
USFDA preapproval inspection at FTO-SEZ PU-01 in Srikakulam resulted in Form 483 with 5 observations; company has responded to the agency and is working to resolve outstanding items.
PSA Segment Softness
PSAI revenue $92m, down 5% YoY and 15% QoQ; PSA reported gross margin of 17.3%, indicating lower profitability and continued pricing pressure in unbranded generics.
Elevated SG&A and Working Capital
SG&A rose 12% YoY to INR 2,692 crore (~31% of revenue), higher by 199 bps YoY (82 bps QoQ) driven by investments in branded franchises, NRT integration, forex impacts and the one-time provision. Operating working capital increased by INR 811 crore QoQ to INR 14,142 crore.
Uncertainty on Pricing and Competition for Semaglutide
While approval momentum exists, management expects more competitive pricing versus initial estimates and acknowledges likely lower-end pricing in many markets; competitive dynamics (e.g., incumbent strategies) could pressure returns.
Company Guidance
The management reiterated clear near‑term and medium‑term guidance: underlying EBITDA should be about 25% (Q3 adjusted was 24.8%), R&D spend is guided at 7–8% of revenues (Q3 R&D was INR 615 crore, ~7% of revenue, 6.8% ex one‑offs), and SG&A (Q3 INR 2,692 crore) is expected to moderate from the current ~30% of revenue excluding one‑offs (Q3 reported ~31%) with any structural labor‑code impact likely <50 bps; gross margin for Global Generics/PSA in a post‑Lenalidomide (from Q4) scenario is expected broadly in the 50–55% range. They confirmed capital and cash metrics (Q3 CapEx INR 669 crore, free cash flow INR 374 crore, operating working capital INR 14,142 crore, net cash surplus $342m, annualized ROCE 20.4%) and hedges (USD 481m at INR 89.1–90.3; RUB 2.93bn at RUB1.06). Product and timeline guidance included semaglutide: India launch March 21, Canada expected between Feb–May, Brazil around July, with ~12m‑cartridge capacity initially and filings/partner deals across ~80+ markets; abatacept IV BLA filed (Dec‑2025) with US launch targeted end‑calendar 2026 and sub‑cut filing in July 2026 (patent expiry/launch ~Jan/Feb 2028) and Europe launch ~July 2027; denosumab/rituximab in the U.S. face CRL/inspection timing uncertainty. Other operational notes: underlying base business is growing double‑digit (India organic ~17–18% this quarter, innovation ~10–15% of India sales), NRT integration is ~85% operational with completion by fiscal year‑end, and Aurigene CDMO is expected to scale (management cited ~$100m+ opportunity over 2–3 years).

Dr. Reddy's Laboratories Ltd. Financial Statement Overview

Summary
Strong profitability and solid balance sheet support an above-average financial profile (Income Statement 86; Balance Sheet 84). The key drag is weaker cash-flow quality/cash conversion (Cash Flow 62), which prevents a top-tier score.
Income Statement
86
Very Positive
Profitability remains strong, with TTM (Trailing-Twelve-Months) gross margin ~56% and net margin ~17% (healthy for generics). Revenue growth is positive across periods (TTM shows strong top-line acceleration vs the latest annual pace), and earnings are solid. The main offset is margin compression versus prior years (EBITDA and EBIT margins are lower than FY2024 levels), suggesting a slightly less favorable mix/cost environment despite continued growth.
Balance Sheet
84
Very Positive
The balance sheet looks conservatively positioned with low leverage (TTM debt-to-equity ~0.16) and sizable equity base. Returns on equity are consistently healthy (~17% TTM), supporting quality of earnings. A watch item is that leverage has moved up versus FY2024 (debt increased meaningfully), though it remains well within comfortable levels for the sector.
Cash Flow
62
Positive
Cash generation is positive and free cash flow improved strongly in TTM (Trailing-Twelve-Months) versus the latest annual period, but cash conversion is the weak link: free cash flow is only ~37% of net income in TTM, indicating earnings are not translating into cash at the same rate (potential working-capital/investment drag). Operating cash flow is solid in absolute terms, yet overall cash-flow quality is less consistent than profitability.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue325.54B279.16B245.88B214.39B189.72B
Gross Profit190.43B163.61B139.34B113.84B103.08B
EBITDA88.84B79.29B66.05B47.74B45.71B
Net Income56.54B55.68B45.07B23.57B17.24B
Balance Sheet
Total Assets492.99B387.52B322.85B296.65B265.49B
Cash, Cash Equivalents and Short-Term Investments57.91B81.47B61.80B44.37B34.57B
Total Debt46.77B20.02B13.47B33.84B30.31B
Total Liabilities155.82B106.97B89.99B106.13B90.51B
Stockholders Equity333.39B280.55B230.99B190.53B173.06B
Cash Flow
Free Cash Flow18.92B18.00B40.01B9.06B23.14B
Operating Cash Flow46.43B45.43B58.87B28.11B35.70B
Investing Cash Flow-51.02B-40.28B-41.37B-26.39B-22.66B
Financing Cash Flow11.86B-3.76B-26.86B-2.42B-298.00M

Dr. Reddy's Laboratories Ltd. Technical Analysis

Technical Analysis Sentiment
Neutral
Last Price1280.40
Price Trends
50DMA
1242.82
Negative
100DMA
1250.61
Negative
200DMA
1249.37
Negative
Market Momentum
MACD
-7.11
Negative
RSI
48.84
Neutral
STOCH
67.14
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For IN:DRREDDY, the sentiment is Neutral. The current price of 1280.4 is above the 20-day moving average (MA) of 1209.31, above the 50-day MA of 1242.82, and above the 200-day MA of 1249.37, indicating a neutral trend. The MACD of -7.11 indicates Negative momentum. The RSI at 48.84 is Neutral, neither overbought nor oversold. The STOCH value of 67.14 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Neutral sentiment for IN:DRREDDY.

Dr. Reddy's Laboratories Ltd. Risk Analysis

Dr. Reddy's Laboratories Ltd. disclosed 60 risk factors in its most recent earnings report. Dr. Reddy's Laboratories Ltd. reported the most risks in the "Legal & Regulatory" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Dr. Reddy's Laboratories Ltd. Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
74
Outperform
₹704.11B19.530.33%7.33%-3.79%
72
Outperform
₹982.60B22.500.57%15.49%64.37%
72
Outperform
₹890.72B18.211.19%14.01%14.62%
70
Outperform
₹1.02T17.820.63%14.10%9.72%
68
Neutral
₹1.07T23.460.87%6.93%21.55%
66
Neutral
₹1.34T62.070.84%9.11%18.76%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
IN:DRREDDY
Dr. Reddy's Laboratories Ltd.
1,218.40
8.47
0.70%
IN:AUROPHARMA
Aurobindo Pharma Ltd
1,212.30
44.93
3.85%
IN:CIPLA
Cipla Ltd
1,323.95
-139.75
-9.55%
IN:LUPIN
Lupin Limited
2,151.05
83.10
4.02%
IN:TORNTPHARM
Torrent Pharmaceuticals Ltd
3,959.75
706.72
21.72%
IN:ZYDUSLIFE
Zydus Lifesciences Limited
885.20
-73.81
-7.70%

Dr. Reddy's Laboratories Ltd. Corporate Events

Dr. Reddy’s Publishes Audio Recording of Q3 FY2026 Earnings Call
Jan 21, 2026

Dr. Reddy’s Laboratories has notified stock exchanges that the audio recording of its earnings call for the quarter ended December 31, 2025, held on January 21, 2026, has been made publicly available via a web link on the company’s website. The disclosure, made under Indian listing regulations, enhances transparency for investors and other stakeholders by providing direct access to management’s commentary on quarterly performance and outlook, reinforcing the company’s adherence to corporate governance and disclosure norms.

Dr. Reddy’s Releases Q3 FY26 Unaudited Results Investor Presentation
Jan 21, 2026

Dr. Reddy’s Laboratories Ltd. has released an investor presentation detailing its unaudited financial results for the third quarter of fiscal year 2026, covering the period ended 31 December 2025. The disclosure, made under Indian securities listing regulations, is intended to update shareholders and market participants on the company’s consolidated performance under IFRS and forms part of its regular financial reporting and investor communication practices.

Dr. Reddy’s Gets USFDA Post-Application Action Letter for Hyderabad Biologics Plant
Jan 10, 2026

Dr. Reddy’s Laboratories has received a Post-Application Action Letter from the US Food and Drug Administration following a pre-approval inspection of its biologics manufacturing facility at Bachupally, Hyderabad. The company said it will work closely with the US regulator to address the queries raised, underscoring the importance of resolving these compliance issues for the approval timeline of its biologics products and for maintaining its position in the highly regulated U.S. pharmaceutical market.

Dr. Reddy’s Laboratories Receives USFDA Observations Post-Inspection
Dec 12, 2025

Dr. Reddy’s Laboratories Ltd. announced that the USFDA completed a GMP and Pre-Approval Inspection at its formulations facility in Srikakulam, Andhra Pradesh. The inspection, which took place from December 4 to December 12, 2025, resulted in a Form 483 with five observations. The company plans to address these observations within the stipulated timeline, which is crucial for maintaining its compliance and operational efficiency in the competitive pharmaceutical industry.

Dr. Reddy’s Laboratories to Engage with Investors at Hyderabad Conference
Dec 12, 2025

Dr. Reddy’s Laboratories Ltd. has announced its participation in an upcoming investor conference organized by B&K Securities in Hyderabad. This engagement is part of the company’s ongoing efforts to maintain transparency and engage with institutional investors, which could potentially impact its market positioning and investor relations positively.

Dr. Reddy’s Laboratories Releases Q2 FY26 Earnings Call Transcript
Oct 30, 2025

Dr. Reddy’s Laboratories Ltd. has released the transcript of its earnings call for the quarter and half-year ending September 30, 2025. This disclosure is part of the company’s compliance with regulatory requirements, and the transcript is available on their website. The earnings call, conducted on October 24, 2025, featured key management figures, including the CEO and CFO, discussing the company’s financial performance and strategic outlook. This announcement provides stakeholders with insights into the company’s operational and financial health, potentially impacting investor decisions and market perceptions.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Jan 26, 2026