Onesource Specialty Pharma / Q4-FY26

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Positive2026-04-30Back to ONESOURCESPECIALTYPHARMA

Revenue

₹428 Cr

verified against source

Revenue YoY

reported change

EBITDA

₹91.9 Cr

latest reported figure

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PAT (₹ Cr)PositiveWatchNegative
1 actual records
Actual quarterly PAT (₹ Cr) trajectoryReported values plotted by quarter. Hover or focus a point for its quarter, value, and source sentiment.Q4 FY26: 5 · Positive source sentiment · 2026-04-30Q4 FY2655
Values are taken from the available verified source records; sentiment color is a separate source-read indicator.

Quarter read

What the record says.

Onesource Specialty Pharma delivered a strong Q4 FY26 recovery with revenue of ₹428.2 crore (up 47% QoQ) and EBITDA of ₹91.9 crore (up >5x QoQ), driven by the start of commercial shipments of generic semaglutide drug-device combinations in India and Canada. The company reaffirmed its FY28 guidance of $400 million revenue with ~40% EBITDA margins, supported by capacity expansion (second line online in Q2, third by year-end) and a robust demand pipeline across regulated and emerging markets. Biologics funnel expanded 4x YoY, adding key partnerships. The related-party transaction with Ster Science was deferred due to valuation concerns from minority shareholders. Key risk: any delay in regulatory approvals or capacity ramp-up could temper the sequential growth trajectory.

Colored figures show movement against the previous available record.

Guidance to track

  • Reaffirmed organic revenue guidance of $400 million for FY28, driven by semaglutide DDC and base business growth.
  • Reaffirmed EBITDA margin guidance of approximately 40% for FY28, supported by operating leverage from capacity expansion.
  • The second drug-device combination line is undergoing qualification and will be available for commercial manufacturing from Q2 FY27.
  • A third DDC line will be installed and operational by the end of FY27, bringing total lines to three.

Risks flagged

  • The proposed scheme to acquire Ster Science injectables business was deferred due to valuation concerns from a long tail of smaller investors, despite majority support.
  • Revenue growth relies on customers obtaining regulatory approvals in various markets; delays could impact sequential improvement.
  • New lines must be qualified and validated on time; any delays could constrain ability to meet robust demand.
  • Oral GLP-1 formulations could capture up to a third of the market, potentially reducing demand for injectable formulations.

Key quotes

  • We are the first and the only CDMO partner for the first three generic semaglutide approvals in all the highly regulated markets US and Canada.
  • We decided to defer this transaction until such time both One Source delivers on its 400 million and the incoming assets deliver on its 40 million of EBIT.
  • The biggest challenge actually for the customers is access to capacity... customers have done a capacity reservation with us including take or pay kind of contract.

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