S

Symbiotec Pharmalab Ltd.

BSE
ListedListed on 1 Sept 2026-1.0%

₹938–988

₹ 1,297 Cr

15 Shares

₹ 14,070

₹2

Financial Summary

Consolidated(in ₹ million)
ParticularsFY 2025-26FY 2024-25
8,691.497,515.54
31.0944.25
8,722.587,559.79
6,304.795,488.36
1,533.631,469.75
1,099.03967.85

Subscription Details

71.26xTotal
Subscription
12.96x
73.63x
172.03x
15.41x

IPO Timeline

IPO Offer Start

24 Aug 2026

IPO Offer Ends

27 Aug 2026

1 Sept 2026

Use of Proceeds

#PurposeAmount (₹ Million)
1Prepayment and/or repayment, in full or in part, of all or a portion of certain outstanding1,125
2General corporate purposes295.25

Promoters

Anil SatwaniKashish SatwaniSushil SatwaniSatwani Holdings LLP

Book Running Lead Managers

JM Financial Ltd.Avendus Capital Pvt Ltd.Motilal Oswal Investment Advisors Pvt LtdNomura Financial Advisory & Securities (India) Pvt Ltd.

Promoter Shareholding

Pre-IPO

34.47%

Promoter stake

Post-IPO

33.28%

Promoter stake

Offered to Public

1,31,24,929

shares

Post Share Capital

2,13,83,823

shares

About the Company

We are a research and development-driven, science-based pharmaceutical and biotechnology company with capabilities across three platforms- organic chemistry, biotechnology and complex injectables. We have a global leadership position in corticosteroid and steroidal-hormone active pharmaceutical ingredients (“APIs”) in volume terms in Fiscal 2025, with a global volume market share of 36.2% in corticosteroid and 44.2% in steroidal-hormone APIs. (Source: F&S Report) We are the only Indian and global company to have a presence across the top 10 corticosteroid and steroidal-hormone APIs in Fiscal 2025, (Source: F&S Report) demonstrating the depth of our portfolio. We manufacture these products using fermentation and multi-step complex chemical reactions. With over 30 years of industry experience, we have evolved from a lab-scale steroidal-hormone API anufacturer in 1995 into an industrial-scale, backward-integrated platform with approvals from the United States Food and Drug Administration (“US FDA”), European Union Good Manufacturing Practices (“EU-GMP”), Ministry of Food and Drug Safety, Korea and other global organisations. We have leveraged our deep capabilities across organic chemistry,biotechnology, and complex injectables to operate as a contract development and manufacturing organisation (“CDMO”) variably for specialty pharmaceutical and nutraceutical companies globally, offering products and services across the three platforms in which we also manufacture our own products. As of June 30, 2025, we had two operational industrial-scale API manufacturing facilities with a maximum chemical synthesis capacity of 584.67 metric tonnes (“MT”) and fermentation capacity of 300 kilolitres (“KL”). Further, as of the date of this Draft Red Herring Prospectus, we have newly commissioned two additional manufacturing facilities, leading to an aggregate maximum chemical synthesis capacity of 584.67 MT, maximum fermentation capacity of 700 KL, and complex injectables capacity of 20 million vials per annum, enabling us to function as a vertically integrated ‘microbe-topharmacy’ and ‘farm-to-pharmacy’ platform with cost-efficient operations. Our biotechnology facilities are equipped with fermenters of 5 KL, 35 KL and 100 KL, providing us flexibility in the scale of our operations. Further, we are in the process of expanding our biologics capacity by adding a proposed dedicated 14 KL (comprising two reactors of 7 KL each) fermentation capacity for biologics manufacturing in Ujjain.

Use of Proceeds

1. Prepayment and/or repayment, in full or in part, of all or a portion of certain outstanding borrowings availed by our Company; and2. General corporate purposes.