Shilpa Medicare posts record Q1FY27 revenue, eyes consistent growth and better ROCE
Shilpa Medicare reported record Q1FY27 revenue of ₹469 crore (+43% YoY), EBITDA of ₹139 crore (+42%), and PAT of ₹101 crore (~115% growth), with EBITDA margins at 30% and a credit rating upgrade to AA-. The company expects consistent growth with faster profitability and better ROCE, with the tax rate normalizing around 25% in upcoming quarters after a negative rate in Q1 FY27 due to a deferred tax liability reversal. Key pipeline milestones include the first ADC biosimilar set to begin human trials in FY27 and partnerships with Orion Corporation and Gate2Brain.

*this image is generated using AI for illustrative purposes only.
Shilpa Medicare Limited delivered its strongest quarterly performance in Q1FY27, reporting a record revenue from operations of ₹469 crore, a 43% year-on-year increase. The pharmaceutical group's EBITDA rose 42% to ₹139 crore, while net profit after tax (PAT) more than doubled to ₹101 crore. This robust top-line growth was driven by broad-based momentum across its API, Formulations, and CDMO verticals, alongside improved operating leverage that pushed EBITDA margins to 30%. The strong financial outcome coincided with a credit rating upgrade, shifting the company's category from A+ to AA-, validating its strengthening balance sheet.
The results were disclosed via an investor presentation filed with the National Stock Exchange (NSE) and Bombay Stock Exchange (BSE) on August 5, 2026, pursuant to Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015. Management highlighted that the performance reflects the maturation of regulatory and manufacturing investments made over recent years. Looking ahead, the company expects consistent growth with faster profitability and better return on capital employed (ROCE).
Financial Performance Breakdown
The following table summarizes Shilpa Medicare's key financial metrics for Q1FY27:
| Metric: | Q1FY27 Value | YoY Change |
|---|---|---|
| Revenue from Operations: | ₹469 crore | +43% |
| EBITDA: | ₹139 crore | +42% |
| EBITDA Margin: | 30% | — |
| Net Profit After Tax (PAT): | ₹101 crore | ~115% |
The API segment contributed significantly to revenue growth, expanding by approximately 15% year-on-year, underpinned by steady internal demand from the finished dosage formulation (FDF) vertical and broad-based growth in the non-captive portfolio, particularly within the Specialty CDMO division. The Formulations business witnessed explosive growth, with revenue surging over 100% year-on-year. Excluding licensing income, formulations revenue grew 112%, driven by sharp increases in US markets (₹45 crore), Europe (₹57 crore), and domestic sales (₹24 crore), the latter boosted by the commercial traction of NorUDCA.
Tax Rate and Profitability Outlook
The divergence between revenue growth (43%) and PAT growth (~115%) indicates significant operating leverage. With fixed costs remaining relatively stable while high-margin contributions from Specialty CDMO and novel formulations scaled up, every incremental rupee of revenue translated disproportionately into net profit. Notably, the tax rate in Q1 FY27 was negative due to a deferred tax liability reversal; upcoming quarters are expected to see the tax rate normalizing around 25%. The upgrade in credit rating to AA- further suggests that lenders view the company's cash flow generation and balance sheet prudence as materially improved.
Strategic Developments and Pipeline
Beyond financial metrics, Shilpa Medicare advanced several strategic initiatives. The company entered a partnership with Orion Corporation for the co-development and exclusive supply of a nivolumab biosimilar in Europe. Additionally, it secured Gate2Brain as its fourth partnership for a novel asset, taking a stake in the company to serve as its integrated CMC partner for G2B-002, an orphan drug-designated oncology asset for brain cancer. Notably, the company's first ADC biosimilar is set to begin human trials in FY27, marking a significant milestone in its biologics pipeline.
The pipeline remains active with multiple milestones expected in FY27. Key developments include:
- NorUDCA: Launched in India in 3QFY26, with order book visibility for FY27 and expansion into Europe and Rest of World (RoW).
- Rotigotine Transdermal Patch: Received EMA approval; launch planned for FY27 in Europe.
- Recombinant Human Albumin: Phase 3 trials to initiate in India and EU in 1HFY27, with a strategic tie-up with Orion for European commercialization.
- Semaglutide: DMF filing targeted for 1HFY27, with dedicated peptide capacity expansion underway.
- ADC Biosimilar: First ADC biosimilar set to begin human trials in FY27.
On a related development, Unicycive Therapeutics received a Complete Response Letter from the US FDA and aims to refile in Q3. An earnings conference call was held on Wednesday, August 5, 2026, at 16:00 hrs IST, allowing management to discuss these results and future outlook with investors.
Historical Stock Returns for Shilpa Medicare
| 1 Day | 5 Days | 1 Month | 6 Months | 1 Year | 5 Years |
|---|---|---|---|---|---|
| +2.26% | +0.52% | +19.02% | +183.82% | +130.27% | 0.0% |
How will the normalization of the tax rate to ~25% in upcoming quarters impact Shilpa Medicare's net profit margins compared to Q1FY27?
What is the expected revenue contribution timeline for the newly approved Rotigotine Transdermal Patch and NorUDCA in European markets?
How might the partnership with Orion Corporation for the nivolumab biosimilar influence Shilpa Medicare's market share in the European oncology sector?


































