About Haohong Pharmaceutical

Haohong (Qihe) Pharmaceutical Technology Co., Ltd. is located in the High-tech Zone of Qihe County, Shandong Province, adjacent to the Yellow River and within the Jinan Economic Circle, enjoying convenient transportation. The company specializes in the R&D and custom production of innovative active pharmaceutical ingredients (APIs) and pharmaceutical intermediates. It passed the ISO 9001:2015 quality management system certification in 2021, was recognized as a Technology-based Small and Medium-sized Enterprise in 2024, and awarded Innovative Small and Medium-sized Enterprise of Shandong Province in 2025.

Haohong has a high-level R&D team and a full range of analytical testing instruments and methods. At present, its production base in Liaocheng is equipped with 30 sets of 3,000–5,000L reactors, with an annual production capacity of 1,000 tons.

The company focuses on the development of active pharmaceutical ingredients and intermediates for anti-cancer, anti-hepatitis C and anti-diabetic therapies, with an emphasis on high-grade intermediates. Its main products include Bicalutamide, Enzalutamide, Apalutamide, Darolutamide, Abemaciclib, Venetoclax, Macitentan, Empagliflozin, Larotrectinib, Apixaban, Rivaroxaban, Ibrutinib, Ceritinib, Pomalidomide, Lenalidomide, Ivacaftor, Tofacitinib, Cabozantinib, Alectinib, etc.

Our products are exported to overseas markets including the United States, Europe, Japan, India, Bangladesh and other regions. The company currently has dozens of high-grade intermediates available for commercial production, and also provides customers with efficient custom synthesis services ranging from gram scale to hundreds of kilograms.

Adhering to the corporate philosophy of "Pragmatism, Innovation, Integrity", Haohong is committed to serving global customers with full dedication!
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World-Class Team
Graduates from top universities worldwide
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Advanced R&D
Self-developed
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Innovation Focus
Multiple innovative technologies

Our Products

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CAS:1247927-81-6

CAS:1247927-81-6

Model: 8669713543
Parameters: 7739806862

CAS:1207294-92-5

CAS:1207294-92-5

Model: 7458647043
Parameters: 6620579108

CAS:42055-15-2

CAS:42055-15-2

Model: 3-(METHYLAMINO)-1-PROPANOL
Parameters: 1176053477

CAS:100-76-5

CAS:100-76-5

Model: QUINUCLIDINE
Parameters: 4298567087

CAS:770-69-4

CAS:770-69-4

Model: 1-ETHYLADAMANTANE
Parameters: 5846740413

CAS:99-59-2

CAS:99-59-2

Model: 2-Amino-4-nitro anisidine
Parameters: 6983999274

CAS:5398-27-6

CAS:5398-27-6

Model: 2,6-DIIODO-4-NITROANILINE
Parameters: 9718154000

CAS:949-99-5

CAS:949-99-5

Model: 4-Nitro-3-phenyl-L-alanine
Parameters: 9087092423

CAS:80430-23-5

CAS:80430-23-5

Model: 1637513798
Parameters: 2227087315

CAS:35320-23-1

CAS:35320-23-1

Model: (R)-(-)-2-Amino-1-propanol
Parameters: 0505046717

CAS:3048-01-9

CAS:3048-01-9

Model: 1241409617
Parameters: 2488467502

CAS:6960-42-5

CAS:6960-42-5

Model: 7-Nitroindole
Parameters: 7808853291

CAS:13096-62-3

CAS:13096-62-3

Model: 1330534743
Parameters: 1635585104

Abemaciclib Intermediate

Abemaciclib Intermediate

Model: 758997367X
Parameters: 3482092419

Alectinib Intermediate

Alectinib Intermediate

Model: 3241020916
Parameters: 1288336594

Apalutamide Intermediate

Apalutamide Intermediate

Model: 2649993103
Parameters: 9562717054

Company Gallery

Certifications & Awards

Utility Model Patent
Utility Model Patent
Utility Model Patent
Utility Model Patent
Utility Model Patent
Utility Model Patent
Utility Model Patent
Utility Model Patent
ISO 9001:2015 Quality Management System Certificate
ISO 9001:2015 Quality Management System Certificate

Success Stories & Case Studies

Top-tier Pharmaceutical Group

Top-tier Pharmaceutical Group

1High reaction yield reduces the production cost of finished pharmaceuticals.
2Low levels of impurities, heavy metals and residual solvents minimize drug safety risks.
3Stable quality across batches improves the consistency of customers’ pharmaceutical production.
4Simplified downstream synthesis processes shorten drug development cycles.
5Accelerates the drug registration process.
Ultra‑high purity with strictly controlled impurities, heavy metals and residual solvents.
Consistent quality batch‑to‑batch, stable crystal form and particle size.
Strict compliance with ICH, GMP and international pharmaceutical standards.
Stable large‑scale production capacity and reliable supply chain.
Customizable R&D support for API synthesis and drug registration.

Location: US,AE,AU,BD,CA,CN,DE,FR,KR,SA,GB,IN,SG,SE 📦 Quantity: 200

Company & Product Videos

Company Introduction & Factory Tour

⏱ Duration: 3:45 | 👁 Views: 15,230

Product Demonstration - Kestrel K-1

⏱ Duration: 5:12 | 👁 Views: 28,450

Technology Innovation Showcase

⏱ Duration: 4:30 | 👁 Views: 12,890

Customer Testimonials & Success Stories

⏱ Duration: 6:20 | 👁 Views: 9,650

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