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Top Quality Sodium Lactate Ringer Injection 500ml CMP Certified -Huaren Pharmaceutical
US$0.60-0.90
10,000 Bags
Sample price:US$0.00/bag.Request sample
Product profile
Customization
AvailableApplication
Water,Electrolytes and Acid-Base Balance RegulatorUsage Mode
Intravenous DripSuitable for
Elderly, Children, AdultState
LiquidShape
LiquidType
Inorganic ChemicalsPharmaceutical Technology
Chemical SynthesisDrug Reg./Approval No.
H20023794Transport Package
CartonSpecification
500mlTrademark
HuarenOrigin
ChinaKey features
CMP Certified Quality: Product meets CMP certification standards for pharmaceutical safety.
Multiple Specifications: Available in 500ml and 1000ml Non PVC soft bags with single or double valves.
Regulatory Approval: Drug Registration No. H20023794 ensures compliance with medical standards.
Self-Produced Materials: Packaging materials, rubber stoppers, and APIs are self-produced for quality assurance.
GMP Certified Production: All production lines have passed new GMP certification for manufacturing safety.
Flexible Customization: Offers full, minor, and flexible customization from samples or designs.
100% Product Inspection: Finished products undergo 100% visual and function inspection before release.
Established Manufacturer: Huaren Pharmaceutical established in 1998 with 25 years of export experience.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 25 Years CertifiedNearest Port: Qingdao PortAverage Response Time: >24h
AI-Powered supplier vetting
SummaryThe supplier is a limited company founded in 1998, with 559 employees and a 54,736.0 m² manufacturing plant. It operates across pharmaceuticals, APIs, medical devices, medical services, medical supplies, and related production and trading activities. Evidence confirms OEM services for well-known brands, SDK availability, valid manufacturing contracts, quality assurance, raw-material traceability, and documented corrective-action and complaint-handling procedures. The supplier has an effective import/export license and reports overseas service coverage in Russia, but lacks in-stock capacity, overseas warehouses, overseas showrooms, overseas agents or branches, and offline trade-show participation. Financial information is insufficient for a credibility assessment, and no specific customer cases or formal certifications are provided.
Supplier typeThe supplier is identified as a limited company and a combined business, founded in 1998, with activities spanning pharmaceutical and health products, medical devices, manufacturing, processing, and sales. It is not identified as an offshore company and is not part of a larger company group.
After-Sales capabilityThe supplier has documented corrective and preventive action procedures, complaint-handling procedures with records, quality assurance, and raw-material traceability. It can provide overseas services in Russia, but has no overseas agents or branches, overseas warehouse, or overseas showroom, limiting local and inventory-based support.
R&D capabilityThe supplier explicitly reports R&D capability and SDK availability, and describes a strategy involving independent research and collaborative innovation. Its company profile also states that it integrates R&D, production, and sales, supporting a positive assessment of innovation capability.
Production capacityThe supplier operates a 54,736.0 m² manufacturing plant, has 559 employees, and covers pharmaceutical, API, medical-device, medical-supply, textile, and protective-product production activities. Valid manufacturing contracts exist with each related subcontractor, although the supplier reports no in-stock service capacity.
Customization capabilityOEM service for well-known brands is explicitly confirmed, indicating the ability to manufacture according to customer or brand requirements. The supplier also has documented service-capability assessment procedures and 30 qualified service suppliers, but no further details on product-development customization scope are provided.
Product Q&A
Q:What are the available specifications for this injection?
A:
It comes in 500ml and 1000ml Non PVC soft bags, with options for single or double valves.
Q:Is this product suitable for children and the elderly?
A:
Yes, it is suitable for elderly, children, and adults to regulate body fluids and electrolytes.
Q:What is the drug registration number?
A:
The Drug Reg./Approval No. is H20023794.
Q:Does the company offer OEM or ODM services?
A:
Yes, OEM and ODM services are available, including full and minor customization.
Q:What is the lead time for orders?
A:
Peak season lead time is one month, while off-season lead time is within 15 workdays.
Send Inquiry
*To:
Huaren Pharmaceutical Co., Ltd.
Huaren Pharmaceutical Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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