Divi's Laboratories — Q1 FY26
Divis Laboratories reported a strong Q1 FY26 with PAT rising 26.7% YoY to INR 545 crore, driven by robust custom synthesis traction and backward integration benefits.
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Did management answer the analysts?
Every material analyst question, graded on whether management actually answered it — with the verbatim exchange and quantitative claims checked against filed numbers.
Why gross margin lower despite generic/CS mix?
Asked by Tushar Manoharlal
Acknowledged mix change but did not explain why gross margin fell despite mix shift.
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When considering the ratio of generics to custom synthesis of 47% to 53%, it implies that the API business has sort of been more or less flat year-over-year. In fact, it's reduced quarter-over-quarter as well. Given this backdrop, still the gross margin seems to be lower on a quarter-on-quarter basis.
The generic to custom synthesis ratio is 47%, 53% this quarter. The entire thing would actually reflect that the generics business had a higher component in this quarter compared to the custom synthesis. However, we have always maintained the stand that there could be lumpiness...
Details on biocatalysis platform and biologic entry?
Asked by Tushar Manoharlal
Gave vague description but refused to provide any concrete details.
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Certainly, in the opening remarks, Sir commented on Bravo Catalyst in terms of this platform. If you could shed some light in terms of the kind of work that's happening in this aspect.
We are working on biocatalysis. We are working on resins. We are working on several different platforms... At this point, we are more at the pilot stage working with a few of the innovators on how to move forward on this. I'm not at the liberty to speak much more than this.
Clarify generic business percentage and pricing impact on margins.
Asked by Kunal Dhamesha, Macquarie
Clearly answered the percentage and confirmed pricing pressure impact.
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Is the generic business 53% of the revenue this quarter, or is it 47%? ... I think in the opening remarks, we alluded to pricing pressure in the generic business. Is that something that would have impacted the gross margins of generic business this quarter?
Generic business is 47% this quarter. Yes, the pricing pressures are there in the first quarter as well. Apart from that, there are also additional costs that are being incurred by the generic business...
Peptide capacity status and commercialization timeline.
Asked by Kunal Dhamesha, Macquarie
Did not disclose capacity or plant location; deferred to qualification process.
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The second question is on the peptide capacity. Is it now fully functional for us? If you could now share how much is the capacity that we have put up and in which plant, that would be helpful.
In terms of peptide capacity, we have created capacity for both our pilot work and also in terms of commercialization of our customers. As you know, the total process is not that, you know, we just qualify and then we can start supplying. It has to go through a total qualification process...
Kakinada backward integration impact on raw material dependency.
Asked by Kunal Dhamesha, Macquarie
Did not quantify raw material dependency reduction; discussed capacity shift instead.
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The last part is, you know, with Kakinada phase one, let's say if we have to look at a broader level, how much raw material dependency can we reduce? Let's say our FY 2025 raw material consumption was around INR 3,700 crore.
To explain what Kakinada is doing right now, we are seeing a GMP capacity in our existing Unit 1 and Unit 2. There, we were in the past making critical starting materials, raw materials, backward integrating in a GMP facility, which we have moved to Kakinada right now...
Timeline for Kakinada GMP approval and third-party supplies.
Asked by Damayanti Kerai, HSBC
Provided a clear timeline of one to two years for regulatory approvals.
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For Kakinada, when do you set the GMP approval to come in, which will enable you to start supplies the way you are doing right now from Unit 1 and Unit 2?
Right now, surgically, what we have done is we have emptied Unit 1 and Unit 2 with all the key starting materials and moved it to Kakinada Unit 3... certain long-forward-looking products... we are qualifying them in Kakinada, and then we will start the process, which will take at least one to two years before we have regulatory approvals in place for Kakinada.
Current capacity utilization and headroom in Unit 1/2.
Asked by Damayanti Kerai, HSBC
Gave specific utilization figure and confirmed headroom.
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Unit 1, Unit 2, with the capacity freed up, what kind of utilization is there right now? How much headroom do you have from current level to push forward?
Currently, our capacity utilization is at 80% this quarter. It has been consistent in the last one year. Even with additional capacity of Kakinada coming into play, we are still at 80% capacity utilization, which is ideal for our organization.
Asset turnover of three dedicated plants and peptide capacity.
Asked by Surya Narayan Patra, PhillipCapital
Refused to provide asset turnover or product nature due to confidentiality.
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In terms of the asset turnover, it would be similar to the kind of existing line of asset turnover work we are having for our plants. Any of these three unit adds are relating to peptide or compound material?
There are three projects. I'm not at the liberty to talk too much about it, but the three projects are going as per schedule. They have long-term contracts with volume commitment.
When will generic pricing stabilize and what gives confidence?
Asked by Neha, Bank of America
Did not provide concrete factors or timeline for stabilization; cited hope.
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Nilima ma'am made a comment about probably pricing stabilizing in the next few quarters. If you could just give some color, you know, what essentially would help stabilize this price?
If you look at the inbox comment, it's basically that we are hoping it will stabilize. The pricing pressure is basically because of several geopolitical situations happening across the world... That being said, we being backward integrated... we are able to sustain and have continued supply and we are successful in not losing any market share.
Impact of Valsartan going generic on shipments and guidance.
Asked by Shyam Srinivasan, Goldman Sachs
Declined to comment on specific product citing confidentiality.
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It's gone generic in the U.S., as many may be aware, in the middle of July. I just want to understand, how is our shipments going to vary on the path forward for Valsartan, Acrobyl Valsartan specifically?
Firstly, I cannot acknowledge any products, so I cannot answer this question to be fair. What I can say is every brand company has their own strategy, and we will abide by what the brand requires... If you're talking about late life cycles, we do manage late life cycles with our customers.
Stage of three recently signed projects (clinical/commercial).
Asked by Abdulkader Puranwala, ICICI Securities Limited
Gave qualitative stage but no specifics on molecules or timelines.
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If you could help us understand on the three projects you have recently signed, just qualitatively, if you could indicate at what stage these projects should be, whether this should be something like a molecule under clinical trial or something which is already commercialized?
Just to give you an idea, all the three molecules, some are just commercialized, some of them are commercialized, and when it's in the patents. These are not, and some, you know, they just completed phase three going forward.
New product pipeline timeline for generic segment.
Asked by Speaker 17, Marcellus Investment Managers
Provided specific product names and a clear 6-12 month timeline for commercial volume.
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Can you please help us with the plan and timelines for the new product pipeline at Divi's reference time? You know, when would these products be launched, and what is the timeline?
Coming to the new product pipeline, we have several products like rivaracetone, figagidilor, all, and a few others already in the pipeline. We find that the DMS validations are completed, and we are waiting for our customers to get their approval so that we can start supplies. We think in the next six to 12 months, we will start seeing some movement of the products on commercial volume.