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Dr. Reddy's Laboratories Ltd (RDY)
NYSE:RDY

Dr Reddy's Laboratories (RDY) AI Stock Analysis

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RDY

Dr Reddy's Laboratories

(NYSE:RDY)

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Outperform 70 (OpenAI - 5.2)
Rating:70Outperform
Price Target:
$15.00
▲(7.22% Upside)
Action:UpgradedDate:01/26/26
The score is driven primarily by strong fundamentals (profitability, growth, and low leverage), tempered by weaker cash-flow conversion. Earnings-call takeaways are moderately positive due to pipeline progress and strong liquidity, but near-term margins and regulatory delays add risk. Technicals are neutral-to-soft and valuation is reasonable with a low dividend yield.
Positive Factors
Conservative balance sheet & strong ROE
Low leverage and consistently strong returns on equity provide durable financial flexibility. This capital efficiency supports funding R&D, M&A, and commercial expansion while absorbing cyclical or regulatory shocks, underpinning sustainable shareholder returns over the medium term.
Diversified commercial growth and pipeline
Broad-based growth across India and emerging markets, plus semaglutide authorization and multi‑market filings, reduce reliance on any single product or region. This diversification and pipeline progress strengthen long-term revenue resilience and expand high-growth addressable markets.
Strong liquidity and active hedging
A net cash surplus, positive free cash flow and sizeable FX hedges provide durable financial headroom. This liquidity supports sustained R&D, capex and integration of acquisitions, and mitigates currency volatility risks that can otherwise impair international revenue and margins.
Negative Factors
U.S. biologics regulatory setbacks
Regulatory inspection failures and CRLs materially delay entry of key biosimilars into the U.S. market. Such timing setbacks compress near‑term revenue and push out ROI on biologics investments, highlighting execution and third‑party manufacturing risk for long‑term biosimilars growth.
Weak cash conversion / higher working capital
Earnings are less reliably converted into cash due to rising working capital and capex intensity. Persistent weaker cash conversion reduces financial flexibility, constrains reinvestment or dividends, and increases sensitivity to funding needs during product launches or regulatory delays.
Margin pressure & elevated SG&A
Sustained margin compression and higher SG&A from strategic investments and one‑offs suggest structural profitability headwinds. Combined with U.S. generics price erosion and product mix changes, this can limit long‑term margin sustainability and reduce free cash flow generation.

Dr Reddy's Laboratories (RDY) vs. SPDR S&P 500 ETF (SPY)

Dr Reddy's Laboratories Business Overview & Revenue Model

Company DescriptionDr. Reddy's Laboratories Limited, together with its subsidiaries, operates as an integrated pharmaceutical company worldwide. It operates through Global Generics, Pharmaceutical Services and Active Ingredients (PSAI), Proprietary Products, and Others segments. The company's Global Generics segment manufactures and markets prescription and over-the-counter finished pharmaceutical products that are marketed under a brand name or as a generic finished dosages with therapeutic equivalence to branded formulations. This segment also engages in the biologics business. The PSAI segment manufactures and markets active pharmaceutical ingredients and intermediates, which are principal ingredients for finished pharmaceutical products. This segment also provides contract research services; and manufactures and sells active pharmaceutical ingredients and steroids in accordance with the specific customer requirements. Its Proprietary Products segment focuses on the research and development of differentiated formulations. The Others segment engages in developing therapies in the fields of oncology and inflammation. The therapeutic categories primarily include gastro-intestinal, cardiovascular, anti-diabetic, dermatology, oncology, respiratory, stomatology, urology, and nephrology. The company has a collaboration, license, and option agreement with Curis, Inc. to discover, develop, and commercialize small molecule antagonists for immuno-oncology and precision oncology targets. Dr. Reddy's Laboratories Limited was incorporated in 1984 and is headquartered in Hyderabad, India.
How the Company Makes MoneyDr Reddy's Laboratories generates revenue through multiple streams. The primary source of income is from the sale of generic pharmaceuticals, which are marketed under its own brand names and sold in various markets worldwide. The company also earns significant revenue from proprietary products, including branded formulations and biosimilars. Additionally, the sales of API to other pharmaceutical companies and contract manufacturing services contribute to its earnings. Strategic partnerships and collaborations with other companies enhance its research capabilities and market reach, further boosting revenue. The company’s investments in R&D enable it to introduce new products and maintain a competitive edge, which is essential for sustaining its growth and profitability.

Dr Reddy's Laboratories Earnings Call Summary

Earnings Call Date:Jan 27, 2026
(Q3-2026)
|
% Change Since: |
Next Earnings Date:May 08, 2026
Earnings Call Sentiment Positive
The call reflects a mixed but overall constructive picture: the company demonstrated resilient top-line growth (+4.4% YoY) driven by strong performance in India and emerging markets (double-digit growth) and meaningful pipeline and commercial milestones (semaglutide authorization in India, abatacept filings, European denosumab approval). Liquidity remains healthy (net cash surplus ~USD 342m) and integration of acquisitions is progressing. Offsetting these positives are margin compression, profit declines, continued U.S. generics weakness due to Lenalidomide decline, regulatory/inspection-related delays for some biosimilars (denosumab, rituximab) and elevated SG&A driven by strategic investments and a one-time labor-code provision. On balance the positive operational momentum, pipeline progress and strong cash position modestly outweigh the near-term margin and regulatory challenges.
Q3-2026 Updates
Positive Updates
Revenue Growth and Base Business Momentum
Consolidated Q3 FY'26 revenue INR 8,727 crores (USD 971m), up 4.4% YoY (down 0.9% QoQ). Underlying base business excluding Lenalidomide delivered double-digit growth, aided by favorable forex.
Strong India and Emerging Markets Performance
India revenue INR 1,603 crores, +19% YoY (+2% QoQ); organic India growth ~17-18% excluding Stugeron. Emerging markets revenue INR 1,896 crores, +32% YoY and +15% QoQ; Russia grew ~21% YoY (constant currency). India outperformed IPM (MQT 12.3% vs IPM 11.8%; MAT 9.7% vs IPM 8.9%).
Pipeline and Strategic Regulatory Progress
Key regulatory and pipeline milestones: semaglutide injection received marketing authorization in India and local manufacturing license (India launch planned Mar 21); semaglutide filings underway across emerging markets and response submitted to Health Canada (goal date by May). Abatacept IV BLA filed (Dec 2025) and subcutaneous filing planned Jul 2026; European launch plans for abatacept targeted around Jul 2027.
Biologics and Biosimilars Approvals / Launches in Europe
Denosumab biosimilar received CHMP positive opinion and European Commission approval; MHRA (UK) approval received and product launched in Germany with preparations for U.K. and other European launches.
Cash Generation and Strong Liquidity
Free cash flow for the quarter INR 374 crores (USD 42m); capex INR 669 crores (USD 75m). Net cash surplus INR 3,069 crores (USD 342m) as of Dec 31, 2025. Active FX hedges: USD 481m hedged at INR 89.1–90.3 and RUB 2.93bn at fixed rate.
Commercial Execution and New Product Launches
Launched 30 new products across emerging markets, 10 new generics in Europe, 6 new products in North America during the quarter, and introduced 2 new brands in India; 31 Drug Master Files filed globally and 28 global generic filings completed.
Acquisition Integration and Consumer Health
Integration of acquired Nicotine Replacement Therapy (NRT) business progressing per plan with ~85% of business by value under operational control; NRT delivered overall reported growth (~25% YoY) with constant currency growth ~8% YoY and EBITDA at or above targeted ~25% range.
Sustainability and CDMO/Innovation Progress
Committed to a science-based net-zero target by FY2045 (first Indian pharma with such a commitment) and leadership in CDP Water Security & Climate categories; Aurigene (APSL) served as exclusive API manufacturer for 2 novel USFDA-approved drugs in 2025 and delivered 3 discovery programs via Aurigene.Ai.
Negative Updates
Margin Compression and Profit Declines
Consolidated gross margin 53.6%, down 505 bps YoY and 104 bps QoQ; reported EBITDA margin 23.5% (adjusted 24.8% excluding one-time labor-code provision). EBITDA INR 2,049 crores (USD 228m), down 11% YoY and 13% QoQ. PAT INR 1,210 crores (USD 135m), down 14% YoY and 16% QoQ; diluted EPS INR 14.52.
North America Generics Weakness (Lenalidomide Impact)
North America generics revenue $338m, down 16% YoY and 9% QoQ, primarily due to lower Lenalidomide contribution and ongoing price erosion in U.S. generics. Management indicated Lenalidomide contribution will be materially reduced from Q4 onward.
Regulatory/Inspection Setbacks for Biologics
USFDA inspections resulted in Form 483 with 5 observations at FTO-SEZ (Srikakulam) and a post-application action letter related to rituximab; partner Alvotech received a CRL for denosumab BLA tied to a pre-license inspection of Alvotech's facility, creating potential delays (management indicated denosumab US timing uncertain and possibly into FY'27; rituximab reinspection and delay >6 months possible).
Rising SG&A and One-Time Labor-Code Provision
SG&A INR 2,692 crores (USD 300m), +12% YoY and +2% QoQ; SG&A was ~31% of revenue (+199 bps YoY). Management noted a one-time provision related to changes from new labor law codes (analyst-reference ~INR 117 crores in Q&A) and expects a modest ongoing structural impact (management estimate <50 bps).
PSA/Other Segment Softness
PSAI business revenue $92m, down 5% YoY and 15% QoQ. Global generics and PSA gross margin guidance without Lenalidomide expected to settle around 50–55%, implying margin pressure from historical levels.
Working Capital Increase
Operating working capital as of Dec 31, 2025 increased to INR 14,142 crores (USD 1.57bn), up INR 811 crores QoQ, indicating higher capital tied up in operations.
Company Guidance
Management reiterated forward guidance of R&D at 7–8% of revenues and an underlying EBITDA margin of about 25% (Q3 adjusted 24.8% vs reported 23.5%), with post‑Lenalidomide gross margins for global generics/PSA guided to a 50–55% range; Q3 reported metrics were revenue INR 8,727 crore ($971m, +4.4% YoY), EBITDA INR 2,049 crore ($228m), PAT INR 1,210 crore ($135m) and diluted EPS INR 14.52. SG&A was INR 2,692 crore (~31% of revenue, ~30% excluding the one‑off) and management expects moderation in SG&A growth (discretionary spends controlled and SG&A growth to be less than half of revenue growth). Balance‑sheet and cash targets include operating working capital INR 14,142 crore, capex INR 669 crore ($75m) this quarter, free cash flow INR 374 crore ($42m), net cash surplus INR 3,069 crore ($342m) and hedges of USD 481m (at INR ~89.1–90.3) and RUB 2.93bn; pipeline/timing guidance: semaglutide India launch March 21 (Canada Feb–May goal date, Brazil/Turkey ~July; ~12m cartridge capacity, filings in 80+ markets), abatacept IV BLA filed (US target end‑calendar 2026; subcu target Jan/Feb 2028; Europe filing July 2026 with ~12‑month review and a July 2027 launch), while denosumab and rituximab face CRLs/inspections likely pushing US timing into mid‑to‑late FY‑27 or beyond.

Dr Reddy's Laboratories Financial Statement Overview

Summary
Strong profitability and growth supported by a conservative balance sheet (low leverage, solid ROE). The main drag is weaker and less consistent cash-flow conversion versus net income, pointing to working-capital/capex intensity.
Income Statement
82
Very Positive
RDY shows solid top-line momentum, with revenue growing ~13–17% across recent annual periods and accelerating to 128.8% in TTM (Trailing-Twelve-Months). Profitability is strong for the group: net margins improved materially versus FY2022 (~11%) and have remained healthy around ~17–20% in FY2023–TTM. The main offset is some margin compression in the most recent period versus FY2024 (TTM net margin ~17.1% vs ~19.9% in FY2024; EBIT and EBITDA margins also stepped down), suggesting higher costs or mix pressure despite growth.
Balance Sheet
86
Very Positive
The balance sheet looks conservative with low leverage: debt-to-equity remains modest (roughly ~0.06–0.18 historically; 0.16 in TTM (Trailing-Twelve-Months)). Equity has grown meaningfully over time, supporting financial flexibility. Returns on equity are consistently strong (roughly ~17–20% recently; 17.2% in TTM (Trailing-Twelve-Months)), indicating good capital efficiency. A watch item is that absolute debt has risen versus FY2024 and FY2023, though leverage still screens comfortable.
Cash Flow
63
Positive
Cash generation is positive but less consistent than earnings quality would suggest. Operating cash flow is solid in absolute terms and improved in TTM (Trailing-Twelve-Months) versus FY2025, and free cash flow growth is strong in TTM (31.3%). However, cash conversion is on the weaker side: operating cash flow covers a relatively small portion of revenue (about ~0.36–0.47 historically; 0.39 in TTM (Trailing-Twelve-Months)), and free cash flow is only ~26–40% of net income in FY2024–TTM, down sharply from the much stronger FY2023 level (~68%). This points to higher working capital needs or elevated investment/capex in recent periods.
BreakdownTTMMar 2025Mar 2024Mar 2023Mar 2022Mar 2021
Income Statement
Total Revenue345.83B325.54B279.16B245.88B214.39B2.56B
Gross Profit190.84B190.43B163.61B139.34B113.84B1.30B
EBITDA93.77B96.67B88.42B74.43B45.08B534.77M
Net Income56.59B56.54B55.68B45.07B23.57B232.21M
Balance Sheet
Total Assets562.90B492.99B387.52B321.85B292.83B3.63B
Cash, Cash Equivalents and Short-Term Investments82.59B57.91B81.47B61.80B44.37B472.87M
Total Debt67.73B46.77B20.02B13.47B33.84B414.53M
Total Liabilities187.14B155.82B106.97B90.86B102.30B1.26B
Stockholders Equity372.37B333.39B280.55B230.99B190.53B2.37B
Cash Flow
Free Cash Flow24.26B12.03B18.00B40.01B9.06B23.14B
Operating Cash Flow63.11B46.43B45.43B58.88B28.11B35.70B
Investing Cash Flow-52.33B-58.08B-40.28B-41.37B-26.39B-22.66B
Financing Cash Flow-6.12B18.91B-3.76B-26.86B-2.42B-298.00M

Dr Reddy's Laboratories Technical Analysis

Technical Analysis Sentiment
Positive
Last Price13.99
Price Trends
50DMA
13.87
Positive
100DMA
13.94
Positive
200DMA
14.24
Positive
Market Momentum
MACD
0.25
Negative
RSI
69.35
Neutral
STOCH
89.92
Negative
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For RDY, the sentiment is Positive. The current price of 13.99 is below the 20-day moving average (MA) of 14.06, above the 50-day MA of 13.87, and below the 200-day MA of 14.24, indicating a bullish trend. The MACD of 0.25 indicates Negative momentum. The RSI at 69.35 is Neutral, neither overbought nor oversold. The STOCH value of 89.92 is Negative, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Positive sentiment for RDY.

Dr Reddy's Laboratories Risk Analysis

Dr Reddy's Laboratories disclosed 60 risk factors in its most recent earnings report. Dr Reddy's Laboratories 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 Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
78
Outperform
$13.14B28.0616.38%19.61%11.36%
70
Outperform
$11.92B18.860.64%10.63%6.35%
64
Neutral
$4.61B1,032.399.50%
63
Neutral
$39.79B27.8621.37%-0.25%
60
Neutral
$18.50B-21.09%3.99%-6.40%-320.23%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
49
Neutral
$2.01B-38.78-0.65%8.48%-2.55%66.00%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
RDY
Dr Reddy's Laboratories
14.60
1.63
12.52%
VTRS
Viatris
16.08
5.38
50.28%
NBIX
Neurocrine
131.15
13.56
11.53%
PRGO
Perrigo Company
14.41
-9.16
-38.85%
TEVA
Teva Pharmaceutical
33.62
16.84
100.36%
AMRX
Amneal Pharmaceuticals
14.58
6.15
72.95%

Dr Reddy's Laboratories Corporate Events

Dr. Reddy’s Russian Subsidiary Faces VAT Reclassification Penalty Deemed Immaterial
Jan 26, 2026

On January 23, 2026, Dr. Reddy’s Laboratories LLC, Russia, a step-down wholly owned subsidiary of Dr. Reddy’s Laboratories Limited, received a tax audit decision from the Interdistrict Inspectorate of the Federal Tax Service of Russia, which reclassified certain marketing services as taxable services subject to value added tax (VAT). The Russian tax authority has imposed a penalty of RUB 20.09 million (approximately INR 24.50 million), but Dr. Reddy’s has stated that, based on its evaluation, the matter is not expected to have a material impact on the group’s financials, operations or other activities, and the company plans to submit an appropriate reply to the authority.

The most recent analyst rating on (RDY) stock is a Buy with a $15.00 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Launches First-to-Market Generic of Extra-Strength Pataday in U.S. OTC Eye-Care Segment
Jan 15, 2026

On January 14, 2026, Dr. Reddy’s Laboratories announced it had launched in the U.S. market an over-the-counter Olopatadine Hydrochloride Ophthalmic Solution USP, 0.7%, the first-to-market generic equivalent of Extra Strength Pataday Once Daily Relief, following approval by the U.S. Food and Drug Administration. The antihistamine eye drop, indicated for temporary relief of itchy eyes caused by allergens such as pollen, ragweed, grass, animal hair and dander, expands Dr. Reddy’s existing OTC eye-care portfolio, which already includes 0.2% and 0.1% olopatadine formulations; the move strengthens the company’s store-brand offering with U.S. retailers in a category where the Pataday brand generated about $69.9 million in U.S. sales in the 52 weeks to December 27, 2025, underscoring a meaningful new revenue opportunity and reinforcing its competitive positioning in the U.S. OTC market.

The most recent analyst rating on (RDY) stock is a Buy with a $15.00 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Receives USFDA Post-Application Action Letter for Bachupally Biologics Facility
Jan 12, 2026

On January 10, 2026, Dr. Reddy’s Laboratories disclosed that, following a pre-approval inspection by the U.S. Food and Drug Administration (USFDA) at its biologics manufacturing facility in Bachupally, Hyderabad conducted in relation to a product application referenced in an earlier communication on September 13, 2025, the company has now received a Post-Application Action Letter (PAAL) from the USFDA concerning its submitted response. The drugmaker said it will work closely with the US regulator and is committed to addressing the queries raised in the PAAL, indicating that timelines for approval of the related biologic product could depend on how swiftly and satisfactorily these issues are resolved, an outcome that may influence its near-term US biologics pipeline and regulatory risk profile for investors and other stakeholders.

The most recent analyst rating on (RDY) stock is a Hold with a $15.00 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s to Announce Q3 FY26 Results and Host Earnings Call on January 21, 2026
Jan 9, 2026

On January 8, 2026, Dr. Reddy’s Laboratories announced that it will release its financial results for the quarter and nine months ended December 31, 2025 (Q3 FY26) on Wednesday, January 21, 2026, following a meeting of its board of directors. The company will also hold an earnings call on January 21, 2026 at 19:30 IST / 9:00 ET, with related materials including a press presentation, call audio and transcript to be made available via stock exchanges and the company’s website, providing investors and other stakeholders structured access to management’s discussion of recent financial performance.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Faces GST Penalty Orders for FY 2018–23, Sees No Material Financial Impact
Jan 2, 2026

On January 1, 2026, Dr. Reddy’s Laboratories disclosed that it has received five separate orders from the Goods and Services Tax (GST) Authority, specifically from the Joint Commissioner in the Office of the Principal Commissioner of Central Tax, Visakhapatnam, covering financial years 2018-19 to 2022-23. The orders, dated and received on December 31, 2025, allege that the company availed excess input tax credit under the APGST Act 2017 and impose penalties totaling several hundred million rupees across the five years. Dr. Reddy’s stated that, based on its evaluation, the demands and penalties are not expected to have a material impact on its financials, operations or other activities, and the company is considering filing an appeal with the appellate authority, signaling a potential tax dispute but limited immediate operational or balance sheet risk for stakeholders.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Faces FDA Setback on AVT03 Denosumab Biosimilar After Manufacturing Inspection
Dec 31, 2025

On December 31, 2025, Dr. Reddy’s Laboratories disclosed that its wholly owned Swiss subsidiary received a Complete Response Letter from the U.S. Food and Drug Administration for the Biologics License Application for AVT03 (denosumab), a proposed biosimilar to Prolia and Xgeva developed by Alvotech. The FDA’s response is tied to observations from a pre-license inspection of Alvotech’s manufacturing facility in Reykjavik, signaling that approval of this important biosimilar candidate for the U.S. market will be delayed until the inspection issues are resolved, potentially impacting the timing of Dr. Reddy’s entry into the denosumab biosimilar space and related revenue expectations.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Schedules January 21 Board Meeting to Review Q3 FY26 Results, Closes Trading Window
Dec 23, 2025

On December 23, 2025, Dr. Reddy’s Laboratories announced that its Board of Directors will meet on January 21, 2026 to consider and approve the company’s unaudited standalone and consolidated financial results for the quarter ended December 31, 2025. In line with securities regulations on insider trading, the company also disclosed that its trading window for dealing in its securities will be closed from December 25, 2025 to January 23, 2026, temporarily restricting trades by designated persons ahead of the quarterly earnings announcement and underscoring its compliance focus for investors across its Indian and U.S. listings.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories to Engage with Investors at Chennai Conference
Dec 16, 2025

Dr. Reddy’s Laboratories announced its participation in an investor conference organized by Investec on December 22, 2025, in Chennai. This engagement reflects the company’s ongoing efforts to maintain transparency and strengthen relationships with institutional investors, potentially impacting its market perception and investor confidence.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories Receives USFDA Observations Post-Inspection
Dec 16, 2025

On December 12, 2025, Dr. Reddy’s Laboratories announced that the United States Food & Drug Administration (USFDA) completed a Good Manufacturing Practice (GMP) and Pre-Approval Inspection (PAI) at its formulations facility in Srikakulam, Andhra Pradesh. The inspection, conducted from December 4 to December 12, resulted in a Form 483 with five observations, which the company plans to address within the stipulated timeline. This inspection and its outcomes are crucial for the company’s compliance and operational integrity, potentially impacting its market positioning and stakeholder confidence.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories Allots Equity Shares Under ESOPs
Dec 10, 2025

On December 9, 2025, Dr. Reddy’s Laboratories announced the allotment of 9,165 equity shares to eligible employees under its Employee Stock Options Schemes of 2002 and 2007. This move is part of the company’s ongoing efforts to reward and retain its workforce, potentially enhancing employee satisfaction and motivation. The issuance of these shares, which are fully paid up and rank pari passu with existing shares, reflects the company’s commitment to its employee benefits programs and could positively impact its operational dynamics and stakeholder relations.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s and Immutep Forge Strategic Partnership for Eftilagimod Alfa
Dec 8, 2025

On December 8, 2025, Dr. Reddy’s Laboratories announced a strategic collaboration and exclusive licensing agreement with Immutep SAS to develop and commercialize Eftilagimod Alfa, a novel cancer immunotherapy, outside North America, Europe, Japan, and Greater China. This agreement allows Dr. Reddy’s to expand its oncology portfolio by leveraging its market access and expertise to advance Eftilagimod Alfa’s development, while Immutep will receive an upfront payment of USD 20 million and potential milestone payments. The collaboration underscores Dr. Reddy’s commitment to delivering innovative cancer treatments and positions the company to enhance its impact in global oncology markets.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories to Engage with Investors at Singapore Conference
Dec 3, 2025

Dr. Reddy’s Laboratories announced its participation in an investor conference organized by Bank of America in Singapore on December 8-9, 2025. This engagement is part of the company’s ongoing efforts to maintain transparency and communication with its investors, potentially impacting its market perception and stakeholder relations.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories to Engage with Investors at Tokyo Conference
Nov 28, 2025

On November 28, 2025, Dr. Reddy’s Laboratories announced its participation in an upcoming investor conference organized by Nomura in Tokyo, Japan, scheduled for December 4-5, 2025. This engagement underscores the company’s proactive approach in maintaining transparency and fostering relationships with institutional investors, potentially impacting its market perception and stakeholder confidence.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Gains EU Approval for Denosumab Biosimilar
Nov 25, 2025

Dr. Reddy’s Laboratories announced on November 24, 2025, that it has received European Commission approval for AVT03, a biosimilar of Prolia® and Xgeva®, which are used to treat osteoporosis and prevent bone complications in cancer patients. This approval, based on comprehensive evidence and clinical trials, allows Dr. Reddy’s to market AVT03 across EU and EEA countries, enhancing its position in the biosimilars market and potentially increasing its market share in Europe and the US, where it holds exclusive commercialization rights.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories Schedules Investor Conferences for November 2025
Nov 18, 2025

Dr. Reddy’s Laboratories announced its participation in several investor conferences scheduled for late November 2025. These meetings, organized by Investec, Citi, and HSBC, will take place in Mumbai, Hyderabad, and Hong Kong, respectively, and involve in-person group meetings with institutional investors. The participation in these conferences underscores Dr. Reddy’s commitment to engaging with investors and providing updates on its strategic initiatives, potentially impacting its market perception and investor relations.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories to Engage with Investors at Mumbai Conference
Nov 17, 2025

On November 17, 2025, Dr. Reddy’s Laboratories announced its participation in an investor conference organized by JM Financial, scheduled for November 21, 2025, in Mumbai. This meeting, which will be conducted in person, aims to engage with investor groups and provide insights into the company’s operations and strategies. The event is significant for stakeholders as it reflects the company’s proactive approach in maintaining transparency and fostering investor relations.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s API Facility Passes USFDA Inspection with Zero Observations
Nov 17, 2025

On November 14, 2025, Dr. Reddy’s Laboratories announced that the United States Food & Drug Administration (USFDA) completed a Good Manufacturing Practice (GMP) inspection at their API facility in Srikakulam, Andhra Pradesh, with zero observations. This successful inspection underscores the company’s commitment to maintaining high-quality standards in its manufacturing processes, potentially strengthening its position in the global pharmaceutical market.

The most recent analyst rating on (RDY) stock is a Buy with a $15.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories Allots Equity Shares Under ESOP
Nov 13, 2025

On November 13, 2025, Dr. Reddy’s Laboratories announced the allotment of 7,430 equity shares to eligible employees under its Employees Stock Options Scheme, 2002. This move reflects the company’s commitment to employee engagement and retention, potentially enhancing its operational efficiency and stakeholder value.

The most recent analyst rating on (RDY) stock is a Hold with a $14.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Announces Resignation of Global Head of Biologics
Nov 12, 2025

Dr. Reddy’s Laboratories announced the resignation of Mr. Jayanth Sridhar, the Global Head of Biologics, effective January 31, 2026. This change in senior management is part of the company’s ongoing adjustments to its leadership team, which could impact its strategic direction in the biologics sector.

The most recent analyst rating on (RDY) stock is a Hold with a $14.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Receives Non-Compliance Notice for Semaglutide Injection in Canada
Oct 29, 2025

On October 29, 2025, Dr. Reddy’s Laboratories received a Notice of Non-Compliance from the Pharmaceutical Drugs Directorate in Canada concerning their Abbreviated New Drug Submission for Semaglutide Injection. The notice requests additional information and clarifications, which the company plans to address promptly. Despite this setback, Dr. Reddy’s remains confident in the quality and safety of their product and is committed to making it available in Canada and other markets as soon as possible. The company appreciates the support of its stakeholders and will provide further updates when appropriate.

The most recent analyst rating on (RDY) stock is a Buy with a $16.50 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Releases Q3 2025 Earnings Call Recordings
Oct 27, 2025

On October 25, 2025, Dr. Reddy’s Laboratories announced the availability of audio recordings from their earnings call conducted on October 24, 2025. This call covered the financial results for the quarter ending September 30, 2025. The release of these recordings is part of the company’s commitment to transparency and regulatory compliance, providing stakeholders with insights into their financial performance and strategic direction.

The most recent analyst rating on (RDY) stock is a Buy with a $16.00 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

Dr. Reddy’s Laboratories Releases Q2 2025 Financial Results
Oct 27, 2025

On October 25, 2025, Dr. Reddy’s Laboratories announced the publication of its unaudited financial results for the quarter and half-year ending September 30, 2025. These results were advertised in the Financial Express and Andhra Prabha newspapers. This disclosure is part of the company’s compliance with the Securities and Exchange Board of India’s regulations, reflecting its commitment to transparency and providing stakeholders with timely financial information.

The most recent analyst rating on (RDY) stock is a Buy with a $16.00 price target. To see the full list of analyst forecasts on Dr Reddy’s Laboratories stock, see the RDY Stock Forecast page.

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