Hisun Pharmaceutical 2025 Results: Continued Streamlining, Improving Manufacturing Gross Margin
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Hisun Pharmaceutical 2025 Results: Continued Streamlining, Improving Manufacturing Gross Margin
Morgan Stanley believes Hisun Pharmaceutical is improving earnings by divesting non-strategic businesses and focusing on higher-margin segments; earnings grew after excluding special items in 2025, but API pricing and export contracts remain key risks.
- 2025 revenue was Rmb10.5bn, up 2.0% YoY; attributable earnings were Rmb541mn, down 10.1% YoY, but were 12.9% and 28.8% above Morgan Stanley's estimates, respectively.
- After excluding special items such as 2024 convertible bond gains, 2025 earnings increased 36.1% YoY to Rmb586mn.
- The distribution business was deconsolidated starting in March 2026; on a retrospective basis excluding the distribution business, revenue increased from Rmb7.1bn to Rmb7.6bn, up 6.4% YoY.
- Manufacturing revenue grew 7.5% YoY, and gross margin improved by 1.3ppt to 61.6%; although the API business faced pricing pressure, cost optimization lifted gross margin by 4.2ppt to 33.0%.
Report interpretation
Overview
This report is Morgan Stanley's commentary on Zhejiang Hisun Pharmaceutical Co. Ltd. (600267.SS) 2025 results. The report focuses on the company's operating performance after continued business streamlining, divestment of non-strategic assets, and redeployment of resources toward higher-margin businesses. Revenue grew modestly in 2025 and reported earnings fell, but earnings increased meaningfully after excluding special items, while manufacturing gross margin improved.
Core views
The core view is that Hisun Pharmaceutical is improving earnings quality by selling the distribution business and optimizing its business mix. In 2025, the finished-dosage, veterinary drug, oncology, and cardiovascular segments performed well, and overseas revenue growth outpaced the China market; meanwhile, the API business still faces pressure from declining global average selling prices. Future earnings leverage will depend on prescription-drug sales, API pricing, the innovative-drug pipeline, and progress toward the BioRay IPO.
Analysis framework
The report primarily uses company-disclosed data and Morgan Stanley's ModelWare framework to break down revenue, earnings, business segments, product categories, therapeutic areas, regional growth, and gross margin changes, and it explains the target price using a DCF valuation framework.
Methodology notes
Discounted cash flow valuation
The price target is derived from a discounted cash flow analysis, assuming a cost of equity of 8.8%, a perpetual growth rate of 3%, a long-term ROE of 10% on new investment, and a net debt-to-equity ratio of 40%.
Internal model framework
Unless otherwise noted, the report's metrics are based on Morgan Stanley's ModelWare framework.
Overweight、Equal-weight、Not-Rated、Underweight
Morgan Stanley uses a relative rating system, which typically measures risk-adjusted total return over the next 12 to 18 months relative to the covered universe.
Asset mapping & comparison
Structured mapping from thesis to named assets (strengths, weaknesses, peers, risks).
- 600267.SSCovered name in the report
- Strengths
- The company is continuing to divest non-strategic businesses, manufacturing gross margin is improving, and earnings grew YoY after excluding special items, with finished pharmaceuticals and veterinary drugs becoming the main growth drivers in higher-margin areas.
- Weaknesses
- Reported earnings declined YoY, the API business still faces global pricing pressure and export competition, and revenue in infectious disease therapeutics fell.
- Comparison
- 2025 revenue and earnings were respectively 12.9% and 28.8% above Morgan Stanley's estimates; excluding the distribution business, revenue grew 6.4% YoY, and manufacturing revenue grew 7.5% YoY.
- Risks
- API price volatility, further delays in Pfizer product supply, loss of export contracts, overseas regulatory export bans, asset impairment, and additional borrowing to support R&D.
Key data
- 2025 revenueRmb10.5bnUp 2.0% YoY and 12.9% above Morgan Stanley's estimate.
- 2025 earningsRmb541mnDown 10.1% YoY and 28.8% above Morgan Stanley's estimate.
- 2025 earnings excluding special itemsRmb586mnUp 36.1% YoY after excluding special items such as 2024 convertible bond gains.
- 4Q25 revenueRmb2,627mnUp 37.4% YoY.
- 4Q25 earningsRmb80mnDown 12.8% YoY.
- Revenue excluding the distribution business on a retrospective basisRmb7.6bnRose from Rmb7.1bn to Rmb7.6bn, up 6.4% YoY.
- Manufacturing revenue growth+7.5% YoYMainly driven by finished pharmaceuticals and veterinary drugs.
- Manufacturing gross margin61.6%Up 1.3 percentage points YoY.
- API gross margin33.0%Up 4.2 percentage points YoY as cost structure optimization offset downward pressure on global pricing.
- Finished pharmaceuticals gross margin68.4%Broadly stable YoY.
- Finished pharmaceuticals revenue growth+9.2%By product category.
- API revenue growth+0.8%By product category.
- China revenue growth+2.4%By region.
- Export revenue growth+11.6%By region.
- Therapeutic area revenue growthOncology +15.1%, infectious diseases -7.3%, cardiovascular +15.5%, antiparasitic and veterinary drugs +22.4%, endocrinology +5.5%The therapeutic-area breakdown shows a differentiated set of growth drivers.
- Distribution business saleRmb501mnOn 2026-03-03, the company completed the sale of its Zhejiang provincial distribution business to Guangzhou Pharmaceutical.
Impact & implications
Business streamlining should help improve Hisun Pharmaceutical's revenue quality and margins, especially once the distribution business is no longer consolidated, making it easier for the market to observe the real growth and profitability of the manufacturing core business. If finished pharmaceuticals, veterinary drugs, and higher-margin therapeutic areas continue to expand while API pricing pressure eases, earnings leverage could improve; conversely, lost export contracts, regulatory export bans, asset impairments, or rising funding needs for R&D could weigh on valuation.
Risks
- Further delays in Pfizer product supply.
- Loss of API export contracts due to competition.
- Export bans imposed by overseas regulators.
- Asset impairment losses.
- Additional borrowing to support ongoing R&D.
- Continued decline in global average API selling prices.
What to watch
- Whether API prices in export markets rise sharply.
- Whether prescription-drug sales in China outperform expectations.
- Progress on the innovative-drug pipeline.
- Whether the biotech subsidiary BioRay can successfully list.
- The sustainability of revenue and gross margin in the manufacturing core business after the distribution business divestment.
- Changes in API export contracts and overseas regulatory policies.