Yes, we are a professional manufacturer of pharmaceutical excipients established in January 2010, officially named Shandong Liaocheng Huayang Pharmaceutical Excipients Co., Ltd. We have our own Huayang Pharmaceutical Industrial Park covering an area of 20,000㎡, with fully automated production lines and inspection equipment designed and built in accordance with GMP standards. We are not a trading company, so we can directly control product quality and delivery schedules to provide stable supply for our customers.
We have obtained a series of authoritative certifications and honors to meet global regulatory requirements, including:
All our products comply with the standards of the Chinese Pharmacopoeia (ChP 2020/2025 editions), and relevant certification documents can be provided upon your request.
Our fully automated production lines enable stable annual production capacity for core products: the annual output of corn starch (pharmaceutical grade) exceeds 3,000 tons, and the annual output of dextrin (pharmaceutical grade) exceeds 2,500 tons. Over the years, we have served well-known domestic pharmaceutical groups such as Jianmin Pharmaceutical Group, CSPC Group, and Jichuan Pharmaceutical Group. We have sufficient production capacity to meet large-volume orders from overseas markets, and the delivery cycle can be flexibly adjusted according to the order quantity.
Our core products mainly cover two categories, with clear application scenarios in the pharmaceutical field:
he four models of corn starch are differentiated by core properties such as moisture content, particle size, and microbial limits, and are suitable for different pharmaceutical scenarios:
FBD-A (Ordinary) | Basic adaptability, moisture loss 7.0%-8.0% | General tablets (as excipient/diluent) and capsule filling; used with powdered sugar/dextrin to increase tablet hardness
|FBD-B (Low-moisture) | Good fluidity, moisture loss 4.0%-7.0% | Production of moisture-sensitive APIs (tablets, granules, capsules); used as disintegrant in tablets
|FBD-C (Ultra-fine) | Excellent fluidity, 200 mesh (finer particles) | Preparations requiring high fineness (film-coated tablets, pellets); improves preparation uniformity
|FBD-D (Low-bacteria) | Strict microbial limits (aerobic bacteria <100 cfu/g) | Sterile preparations and oral suspensions (e.g., cephalosporins, penicillins) with high microbial control requirements |
You can choose the model based on the sensitivity of APIs to moisture, the fineness requirements of preparations, and microbial control standards. Our technical team can also provide customized recommendations.
Currently, our products are mainly produced in accordance with the Chinese Pharmacopoeia (ChP 2020/2025 editions) (the specific standards are detailed in the product quality standard table). If customers require compliance with USP (United States Pharmacopoeia), EP (European Pharmacopoeia), or BP (British Pharmacopoeia) standards, we can adjust the production process and quality inspection indicators according to the specific versions of the pharmacopoeia required by customers. The adjustment cycle is usually 4-6 weeks, and a pre-production sample test can be provided to confirm compliance before mass production.
The cost of customized packaging will be calculated separately based on the packaging material and specification requirements, and the production cycle will be extended by 3-5 days.
We implement a three-tier quality control system throughout the production process to ensure product quality meets standards:
We attach great importance to product quality complaints and have established a complete after-sales quality guarantee mechanism:
We support various international shipping terms to meet the different needs of customers, and the shipping time varies by destination:
FOB Qingdao | We are responsible for delivering the goods to the port of Qingdao and completing the export customs clearance; the customer is responsible for sea freight and import customs clearance. | North America (Los Angeles): 18-22 days; Europe (Rotterdam): 25-30 days; Southeast Asia (Singapore): 7-10 days
|CIF (Destination Port) | We are responsible for sea freight, insurance, and export customs clearance; the customer is responsible for import customs clearance. | Same as FOB, but the total cycle includes 1-2 days for insurance handling
DAP (Destination Address) | We are responsible for delivering the goods to the customer's designated address (excluding import duties); the customer is responsible for paying import duties. | Add 3-5 days of inland transportation time based on CIF shipping time |
We cooperate with well-known international shipping companies (e.g., Maersk, COSCO) to ensure stable shipping schedules and timely updates of shipment information.
We provide a complete set of customs clearance documents to help customers complete import procedures smoothly. The documents include:
All documents are provided in both Chinese and English, and we can also add specific content required by the importing country (e.g., halal certification, kosher certification) according to customer requirements.
Yes, we have a professional technical support team composed of 10+ senior engineers with more than 5 years of experience in the pharmaceutical excipient industry. We can provide the following technical support:
If the customer has special storage conditions (e.g., long-term storage in a high-humidity environment), we can provide customized packaging (e.g., vacuum packaging) to extend the effective storage time.
After the goods are shipped, we will provide the customer with a shipment tracking package within 24 hours, including:
The customer can also check the shipment status by entering the bill of lading number on the shipping company's official website, or contact our after-sales specialist for updates at any time.
Yes, we are a professional manufacturer of pharmaceutical excipients established in January 2010, officially named Shandong Liaocheng Huayang Pharmaceutical Excipients Co., Ltd. We have our own Huayang Pharmaceutical Industrial Park covering an area of 20,000㎡, with fully automated production lines and inspection equipment designed and built in accordance with GMP standards. We are not a trading company, so we can directly control product quality and delivery schedules to provide stable supply for our customers.
We have obtained a series of authoritative certifications and honors to meet global regulatory requirements, including:
All our products comply with the standards of the Chinese Pharmacopoeia (ChP 2020/2025 editions), and relevant certification documents can be provided upon your request.
Our fully automated production lines enable stable annual production capacity for core products: the annual output of corn starch (pharmaceutical grade) exceeds 3,000 tons, and the annual output of dextrin (pharmaceutical grade) exceeds 2,500 tons. Over the years, we have served well-known domestic pharmaceutical groups such as Jianmin Pharmaceutical Group, CSPC Group, and Jichuan Pharmaceutical Group. We have sufficient production capacity to meet large-volume orders from overseas markets, and the delivery cycle can be flexibly adjusted according to the order quantity.
Our core products mainly cover two categories, with clear application scenarios in the pharmaceutical field:
he four models of corn starch are differentiated by core properties such as moisture content, particle size, and microbial limits, and are suitable for different pharmaceutical scenarios:
FBD-A (Ordinary) | Basic adaptability, moisture loss 7.0%-8.0% | General tablets (as excipient/diluent) and capsule filling; used with powdered sugar/dextrin to increase tablet hardness
|FBD-B (Low-moisture) | Good fluidity, moisture loss 4.0%-7.0% | Production of moisture-sensitive APIs (tablets, granules, capsules); used as disintegrant in tablets
|FBD-C (Ultra-fine) | Excellent fluidity, 200 mesh (finer particles) | Preparations requiring high fineness (film-coated tablets, pellets); improves preparation uniformity
|FBD-D (Low-bacteria) | Strict microbial limits (aerobic bacteria <100 cfu/g) | Sterile preparations and oral suspensions (e.g., cephalosporins, penicillins) with high microbial control requirements |
You can choose the model based on the sensitivity of APIs to moisture, the fineness requirements of preparations, and microbial control standards. Our technical team can also provide customized recommendations.
Currently, our products are mainly produced in accordance with the Chinese Pharmacopoeia (ChP 2020/2025 editions) (the specific standards are detailed in the product quality standard table). If customers require compliance with USP (United States Pharmacopoeia), EP (European Pharmacopoeia), or BP (British Pharmacopoeia) standards, we can adjust the production process and quality inspection indicators according to the specific versions of the pharmacopoeia required by customers. The adjustment cycle is usually 4-6 weeks, and a pre-production sample test can be provided to confirm compliance before mass production.
The cost of customized packaging will be calculated separately based on the packaging material and specification requirements, and the production cycle will be extended by 3-5 days.
We implement a three-tier quality control system throughout the production process to ensure product quality meets standards:
We attach great importance to product quality complaints and have established a complete after-sales quality guarantee mechanism:
We support various international shipping terms to meet the different needs of customers, and the shipping time varies by destination:
FOB Qingdao | We are responsible for delivering the goods to the port of Qingdao and completing the export customs clearance; the customer is responsible for sea freight and import customs clearance. | North America (Los Angeles): 18-22 days; Europe (Rotterdam): 25-30 days; Southeast Asia (Singapore): 7-10 days
|CIF (Destination Port) | We are responsible for sea freight, insurance, and export customs clearance; the customer is responsible for import customs clearance. | Same as FOB, but the total cycle includes 1-2 days for insurance handling
DAP (Destination Address) | We are responsible for delivering the goods to the customer's designated address (excluding import duties); the customer is responsible for paying import duties. | Add 3-5 days of inland transportation time based on CIF shipping time |
We cooperate with well-known international shipping companies (e.g., Maersk, COSCO) to ensure stable shipping schedules and timely updates of shipment information.
We provide a complete set of customs clearance documents to help customers complete import procedures smoothly. The documents include:
All documents are provided in both Chinese and English, and we can also add specific content required by the importing country (e.g., halal certification, kosher certification) according to customer requirements.
Yes, we have a professional technical support team composed of 10+ senior engineers with more than 5 years of experience in the pharmaceutical excipient industry. We can provide the following technical support:
If the customer has special storage conditions (e.g., long-term storage in a high-humidity environment), we can provide customized packaging (e.g., vacuum packaging) to extend the effective storage time.
After the goods are shipped, we will provide the customer with a shipment tracking package within 24 hours, including:
The customer can also check the shipment status by entering the bill of lading number on the shipping company's official website, or contact our after-sales specialist for updates at any time.