AstraZeneca Pharma India imports and markets AstraZeneca's oncology, biopharmaceutical and rare-disease medicines in India, and heads into its Q2 FY 2026-2027 print with the Indian Pharmaceutical Market running at its fastest growth in the series — Q2 FY27 IPM sales up 14.7% YoY. The key things the results will speak to are whether the Q1 pattern of 30% revenue growth alongside a 32% PAT decline normalises, and how the company discloses the ~Rs. 151.20 Cr NPPA Symbicort demand that is now before the Delhi High Court.
| Results date | November 05, 2026 |
|---|---|
| Quarter | Q2 FY 2026-2027 |
| Previous quarter revenue | Rs. 682.89 Cr (Rs. 6,828.9 Mn), +29.75% YoY |
| Previous quarter PAT | Rs. 37.93 Cr (Rs. 379.3 Mn), -32.06% YoY |
| Market cap | Rs. 15,862.5 Cr |
| CMP | Rs. 6,345.0 |
AstraZeneca Pharma India Limited is scheduled to announce its Q2 FY 2026-2027 financial results on November 05, 2026. The results follow the Q1 FY27 filing made on August 10, 2026.
The quarter's central question is whether AstraZeneca India's revenue momentum holds against a fast-growing market while its expense trajectory normalises — Q1 FY27 showed revenue up 29.75% YoY but PAT down 32.06% as total expenses rose 38.60%.
The demand backdrop strengthened through the quarter: IPM value growth ran at 12.1% in July, 10.7-13.0% across provider reads in August, and 17.1% in September, taking Q2 FY27 IPM sales to Rs. 746.1 Bn, up 14.7% YoY, with oncology — 68.08% of the company's Q1 revenue — up 27.5% over the quarter and AstraZeneca itself posting 26.5% monthly domestic value growth in August.
Two in-window Enhertu indication approvals (July 27, 2026 for neoadjuvant HER2-positive breast cancer and August 7-8, 2026 for the adjuvant DESTINY-Breast05 indication) add launch-driven mix on top of that market flow. On costs, the rupee's quarter-average sat materially above the prior year — it closed at 95.96 on September 15, 2026 — a direct headwind for a portfolio imported entirely at related-party transfer prices, while Q1's EBITDA margin of 7.13% was depressed by a Rs. 142.59 Cr inventory drawdown that has room to normalise.
The NPPA Symbicort Turbuhaler demand of ~Rs. 151.20 Cr — roughly 4x Q1 FY27 PAT — hangs over the print, with the Delhi High Court having barred coercive steps until the January 11, 2027 hearing, making any provisioning or deposit disclosure a Q2/H1 question. Management has given no quantified guidance, so the call will likely centre on the margin bridge, NPPA disclosures and therapy-mix detail rather than target scoring.
Growth-profitability divergence and margin bridge: Q1 FY27 showed revenue and profit moving in opposite directions.
NPPA litigation disclosures: Three NPPA matters are live, two with Delhi High Court interim relief.
Therapy-area momentum and launch cadence: Oncology drives roughly two-thirds of revenue; the mix questions are specific.
Leadership transition and Bengaluru exit completion: Senior churn and restructuring tail items remain open.
Guidance and dated pipeline items: There are no quantified targets to score against.
In Q1 FY27, revenue grew 29.75% YoY to Rs. 6,828.9 Mn but PAT fell 32.06% YoY to Rs. 379.3 Mn because total expenses rose 38.60% YoY, outpacing revenue growth. Clinical-trials expense was a notable driver, having jumped 241.49% in FY26 to Rs. 1,066.8 Mn.
NPPA issued a notice dated July 29, 2026 alleging overcharging under DPCO, 2013 on Symbicort Turbuhaler 160/4.5 for May 2016-November 2025, quantified at Rs. 151,19,66,035 (~Rs. 151.20 Cr) including interest — roughly 4x Q1 FY27 PAT of Rs. 37.93 Cr. The Delhi High Court, by order dated October 29, 2026, directed that no coercive steps be taken until the next hearing on January 11, 2027.
Yes — Q1 FY27 revenue rose 29.75% YoY to Rs. 6,828.9 Mn, and FY26 revenue grew 32.59% YoY to Rs. 22,755.8 Mn. Growth is led by Oncology, which was 68.08% of Q1 FY27 revenue and grew 26% YoY, in an Indian pharma market where oncology grew 27.5% over the September quarter.
In FY26 the company launched Lokelma for hyperkalemia and Soliris — India's first anti-complement therapy for aHUS and PNH — and secured 11 regulatory approvals during the year. More recently, CDSCO granted approval on July 27, 2026 for Enhertu in neoadjuvant HER2-positive Stage II/III breast cancer, followed by import-and-sale permission on August 7-8, 2026 for the adjuvant Enhertu indication.
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