Healthcare · NSE: ZYDUSLIFE
Zydus Lifesciences
Q2 FY27 earnings call · Guided by management
Call held 4 Nov 2026 · Read the filing on NSEFiling
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Highlights are read by AI from the company's filing and can contain mistakes. Check the source page linked to each line.
Share price
Results Q2 FY27, as filed · consolidated · ₹ Cr
| Q2 FY27 | Q2 FY26 | YoY | Q1 FY27 | QoQ | |
|---|---|---|---|---|---|
| Revenue | 7,910 | 6,123 | +29.2% | 8,017 | -1.3% |
| EBITDA | 1,895 | 2,016 | -6.0% | 1,929 | -1.8% |
| EBITDA margin | 23.9% | 32.9% | -897 bps | 24.1% | -12 bps |
| One-off items | 1 | -34 | — | -18 | — |
| PBTProfit before tax | 1,234 | 1,687 | -26.9% | 1,307 | -5.5% |
| Net profit | 926 | 1,259 | -26.5% | 940 | -1.5% |
| EPS (₹) | 9.28 | 12.51 | -25.8% | 9.35 | -0.7% |
From the company's own results filing on NSE. Net profit is the owners' share. Growth and the dotted lines are worked out from the filed figures.
Guidance
Medium-term aim: branded business two-thirds of consolidated revenue
Sharvil Patel · Managing Director · p. 5
Medium-term aim: branded business two-thirds of consolidated revenue
“The strategic decisions undertaken over the years and the capabilities built along the way position us well to achieve our medium-term aspirations of branded business to account for two-thirds of our consolidated revenue.”
H2 margin not expected higher as Saroglitazar spend will rise
Sharvil Patel · Managing Director · Q&A · p. 17
H2 margin not expected higher as Saroglitazar spend will rise
“No, but our SARO spend will also go up.”
US: US guided to single-digit constant currency growth on high FY26 base
Sharvil Patel · Managing Director · Q&A · p. 9
US: US guided to single-digit constant currency growth on high FY26 base
“And as I said, we are still guiding for a single digit growth on constant currency terms on the high base of FY26.”
US specialty: No meaningful Saroglitazar revenue in FY28; from FY29, more realistically FY30
Sharvil Patel · Managing Director · Q&A · p. 18
US specialty: No meaningful Saroglitazar revenue in FY28; from FY29, more realistically FY30
“FY28 will not be any meaningful revenue. It will mostly be starting from FY29, but more realistically FY30.”
Vaccines: Vaccines business to double in 3 to 4 years from Rs 450 crore run rate
Sharvil Patel · Managing Director · Q&A · p. 19
Vaccines: Vaccines business to double in 3 to 4 years from Rs 450 crore run rate
“So, in the next 3 to 4 years, we'll definitely double our business from the current annualized run rate of ₹450 crores.”
More figures from the call
“And what we are expecting is that, you know, excluding R&D and the Saro commercialization cost, other expenses would be in the range of ₹2000 to 2050 crores, that kind of a spend that we are expecting on other expenses side.”
“And R&D cost will, as a percentage, we have guided that is around the 8-8.5% but we don't see R&D for us coming down and it will continue to grow because we are investing heavily”
“but I think over a period of time, 70 to 80 million or close to $100 million will be spent on mostly the phase, this clinical, late stage clinical programme.”
“And we have always said that we are comfortable for till one times net debt to EBITDA and that's what we are guiding.”
“I mean, right now we are at capacity. So, we are selling as much as we can make. The demand in the market is 50% more than what is currently served.”
“So, we still believe that the market will grow between 10 to 11% and we will definitely grow at 200 to 400 basis points consistently more than the IPM from the future point of view.”
In short
- 01Q2 FY27 consolidated revenue was Rs 79.1 billion, up 29%, with a 24% EBITDA margin.
- 02Management maintained its FY27 EBITDA margin guidance of 24% plus despite Saroglitazar launch spending.
- 03Saroglitazar US launch is expected in March; commercial spend expected around $100 million a year.
- 04Saroglitazar targets 10-12% patient share by FY30 and 20% eventually; meaningful revenue from FY29-FY30.
- 05US business still guided to single-digit constant currency growth in FY27; FY28 guidance not given.
- 06India branded business expected to grow 200-400 bps above a market seen at 10-11%.
- 07Net debt fell to Rs 5,200 crore from Rs 5,900 crore; comfortable up to 1x net debt to EBITDA.
- 08Transdermal capacity is full; capacity could double in at least a year.
Capex
Uptick in capex cycle and investments
Sharvil Patel · Managing Director · Q&A · p. 17
Uptick in capex cycle and investments
“But as I said, for us also, there is an uptick on the capex cycle as well as all the investments.”
Capacity
Transdermal patches: Transdermal capacity could double, taking at least a year
Sharvil Patel · Managing Director · Q&A · p. 14
Transdermal patches: Transdermal capacity could double, taking at least a year
“It will take at least a year, but we could double our capacity.”
Segments
India branded formulations: India branded formulations grew 19% year-on-year in Q2
Ganesh Nayak · Director · p. 3
India branded formulations: India branded formulations grew 19% year-on-year in Q2
“In India, our branded formulations business sustained market outperformance with a strong 19% year-on-year growth during the quarter.”
India branded formulations: India branded formulations grew 20% in H1 FY27
Ganesh Nayak · Director · p. 3
India branded formulations: India branded formulations grew 20% in H1 FY27
“Growth during H1 FY27 stood at 20% year-on-year.”
India branded formulations: Chronic and sub-chronic share of India portfolio at 56.9%, up 450 bps in four years
Ganesh Nayak · Director · p. 3
India branded formulations: Chronic and sub-chronic share of India portfolio at 56.9%, up 450 bps in four years
“Contribution of chronic and sub-chronic portfolio has increased consistently over the last several years and stood at 56.9% as per AWACS MAT September 2026, an improvement of 450 basis points over the last four years.”
International markets formulations: International markets formulations revenue Rs 10 billion, up 33%
Ganesh Nayak · Director · p. 4
International markets formulations: International markets formulations revenue Rs 10 billion, up 33%
“Building on this momentum, the business reported revenues of ₹10 billion during the quarter, up 33% year-on-year.”
North America: North America revenue Rs 33.1 billion, up 21% YoY and 7% QoQ
Ganesh Nayak · Director · p. 4
North America: North America revenue Rs 33.1 billion, up 21% YoY and 7% QoQ
“North America business, comprising of the United States and Canada delivered strong performance during the quarter with revenues of ₹33.1 billion up 21% year-on-year and 7% quarter-on-quarter.”
Demand
PBC market expanded with more diagnosis and more patients on drugs
Sharvil Patel · Managing Director · Q&A · p. 15
PBC market expanded with more diagnosis and more patients on drugs
“So, the market has expanded faster, both in terms of patients as well as in terms of more patients being put on to the drugs.”
Consumer wellness - domestic: Domestic wellness demand helped by urban recovery and better rural offtake
Ganesh Nayak · Director · p. 4
Consumer wellness - domestic: Domestic wellness demand helped by urban recovery and better rural offtake
“On the domestic front, demand trends indicated sustained positive momentum across categories driven by a steady urban recovery and improving rural offtake.”
Biologics: Keytruda is a $30 billion plus product; biosimilar size depends on launch timing and rivals
Sharvil Patel · Managing Director · Q&A · p. 13
Biologics: Keytruda is a $30 billion plus product; biosimilar size depends on launch timing and rivals
“And specifically on Keytruda, it's a very large biologics, $30 plus billion of revenue. So, depending on the launch and number of competitors, it will be a meaningful launch.”
Transdermal patches: No company can meet transdermal demand quickly; new capacity takes time
Sharvil Patel · Managing Director · Q&A · p. 14
Transdermal patches: No company can meet transdermal demand quickly; new capacity takes time
“Obviously, no companies have capacities to cater to it immediately. And building new capacity also takes time in transdermal.”
Margins and costs
Q2 EBITDA margin 24% despite Saroglitazar US launch investments
Ganesh Nayak · Director · p. 3
Q2 EBITDA margin 24% despite Saroglitazar US launch investments
“Our operating profitability remained robust with an EBITDA margin of 24% despite continued investments towards Saroglitazar launch related activities in the US.”
EBITDA margin 150 bps higher excluding Saroglitazar launch investment
Ganesh Nayak · Director · p. 3
EBITDA margin 150 bps higher excluding Saroglitazar launch investment
“Adjusted for this investment, our EBITDA margin was higher by 150 basis points.”
Saroglitazar commercial spend to grow over next two quarters
Sharvil Patel · Managing Director · Q&A · p. 7
Saroglitazar commercial spend to grow over next two quarters
“So, yes, we continue, we have been continuing to invest from last quarter to this quarter on the commercialization effort and we will also see some growth in the next quarter, next two quarters also for the commercial launch.”
Consumer wellness: Wellness growth weighs on gross margin as its margin is below the 70s
Sharvil Patel · Managing Director · Q&A · p. 9
Consumer wellness: Wellness growth weighs on gross margin as its margin is below the 70s
“So, wellness, when you see such a high growth, obviously, you know, it's gross margin is not in the 70s.”
Some high gross margin products declined, offsetting US gains
Sharvil Patel · Managing Director · Q&A · p. 10
Some high gross margin products declined, offsetting US gains
“The second thing is also that we had also very significant gross margin products that came down.”
Debt and working capital
Net debt to EBITDA at 0.62 times at end of September 2026
Ganesh Nayak · Director · p. 3
Net debt to EBITDA at 0.62 times at end of September 2026
“Our net debt to EBITDA ratio stood at 0.62 times”
Net debt down to Rs 5,200 crore from Rs 5,900 crore
Sharvil Patel · Managing Director · Q&A · p. 17
Net debt down to Rs 5,200 crore from Rs 5,900 crore
“So, from ₹5900 crores, it's come down to ₹5200 crores net debt.”
Acquisitions and new business
US generics: US generics: 4 ANDAs filed, 12 approvals, 5 launches in Q2
Ganesh Nayak · Director · p. 4
US generics: US generics: 4 ANDAs filed, 12 approvals, 5 launches in Q2
“On the US generics front, we filed 4 ANDAs, received 12 approvals and launched 5 new products during the quarter.”
US generics: Launched first generic Riociguat tablets in the US in October 2026
Ganesh Nayak · Director · p. 4
US generics: Launched first generic Riociguat tablets in the US in October 2026
“Recently, in the month of October 2026, we launched the first generic version of Riociguat tablets.”
Biologics: USFDA accepted for review BLA for Keytruda biosimilar from partner Formycon
Sharvil Patel · Managing Director · p. 6
Biologics: USFDA accepted for review BLA for Keytruda biosimilar from partner Formycon
“On the global specialty initiatives front, we achieved an important milestone in our biologics journey with the USFDA accepting for review the BLA for Keytruda biosimilar developed by our partner Formycon.”
Rare disease: Sentynl licensed Alvelestat from Mereo Biopharma
Sharvil Patel · Managing Director · p. 6
Rare disease: Sentynl licensed Alvelestat from Mereo Biopharma
“During the quarter, our wholly owned US subsidiary, Sentynl Therapeutics entered into a licensing agreement with Mereo Biopharma for Alvelestat”
US specialty: Saroglitazar goal date in November; launch expected in March
Sharvil Patel · Managing Director · Q&A · p. 8
US specialty: Saroglitazar goal date in November; launch expected in March
“November is our current goal date and we are, as I said, our current expectation is to launch in March.”
Risks
USFDA inspections: 1 observation at SEZ-II Ahmedabad, 5 at Moraiya
Ganesh Nayak · Director · p. 4
USFDA inspections: 1 observation at SEZ-II Ahmedabad, 5 at Moraiya
“On the operations front, recently, the USFDA inspected our formulations manufacturing facilities at SEZ-II, Ahmedabad and Moraiya which concluded with one observation and five observations respectively.”
US: Mirabegron competition already factored into US numbers
Sharvil Patel · Managing Director · Q&A · p. 9
US: Mirabegron competition already factored into US numbers
“Yeah, so the Mirabegron is factored in already.”
US generics: Cabozantinib exclusivity subject to ongoing patent litigation
Sharvil Patel · Managing Director · Q&A · p. 10
US generics: Cabozantinib exclusivity subject to ongoing patent litigation
“So, there can be other filings, but the whole point on this would be there is a patent litigation going on right now.”
Biologics: Keytruda biosimilar launch depends on IP litigation; Zydus among first filers
Sharvil Patel · Managing Director · Q&A · p. 11
Biologics: Keytruda biosimilar launch depends on IP litigation; Zydus among first filers
“All we can say is we are one of the first filers on the product and we're under review with the FDA. But the launch will depend on the IP litigation.”
US: Moraiya is less than 30% of US revenue, with few filings
Sharvil Patel · Managing Director · Q&A · p. 13
US: Moraiya is less than 30% of US revenue, with few filings
“So, revenue-wise, Moraiya is around less than 30% of the US revenue and we don't have many filings from Moraiya.”
Other
Q2 consolidated revenue Rs 79.1 billion, up 29% year-on-year
Ganesh Nayak · Director · p. 3
Q2 consolidated revenue Rs 79.1 billion, up 29% year-on-year
“We registered consolidated revenues of ₹79.1 billion, up 29% on a year-on-year basis.”
Q2 EBITDA Rs 18.9 billion; net profit Rs 9.3 billion
Ganesh Nayak · Director · p. 3
Q2 EBITDA Rs 18.9 billion; net profit Rs 9.3 billion
“EBITDA for the quarter stood at ₹18.9 billion while net profit for the quarter stood at ₹9.3 billion.”
Saroglitazar Phase II(b) MASH trial met primary endpoint at 52 weeks
Sharvil Patel · Managing Director · p. 6
Saroglitazar Phase II(b) MASH trial met primary endpoint at 52 weeks
“The study successfully met its primary endpoint, demonstrating resolution of steatohepatitis with no worsening of fibrosis at 52 weeks.”
New Saroglitazar PBC Phase III analysis presented at ACG 2026
Sharvil Patel · Managing Director · p. 6
New Saroglitazar PBC Phase III analysis presented at ACG 2026
“The analysis demonstrated consistent biochemical response benefits versus placebo across geographic subgroups, including both the US and non-US patients.”
Approval to start Phase III trial in India for a monoclonal antibody
Sharvil Patel · Managing Director · p. 6
Approval to start Phase III trial in India for a monoclonal antibody
“In the biotech R&D space, we received regulatory approval to initiate Phase III clinical trial in India for one of our important monoclonal antibodies.”
Sources
- Earnings call transcript, Q2 FY27 Filed 7 Nov 2026 · 21 pages
Management's own statements, quoted from its NSE filings. This page was read by AI and can contain mistakes: check the source pages before relying on any figure. No forecast or opinion of ours. Not investment advice.

