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Product profile
Customization
AvailableApplication
Internal MedicineUsage Mode
For oral administrationModel NO.
50MG, 100MGSuitable for
AdultState
SolidShape
TabletType
Biological ProductsPharmaceutical Technology
Chemical SynthesisTransport Package
CartonSpecification
50MG, 100MGTrademark
OEMOrigin
ChinaHS Code
3004909099Production Capacity
5000000boxKey features
GMP Certified Production: Produced in GMP factory with certifications from China and over ten countries' MOH.
OEM Service Available: Supports customization from samples and designs with own brand options.
100% Finished Product Inspection: All products undergo visual and function inspection with uniform instructions.
Established Manufacturer: Operating since 2004 with 126 employees and 21 years of export experience.
Diverse Payment Terms: Accepts T/T, D/P, PayPal, Western Union, and small-amount payments.
Global Shipping Options: Offers FOB, CIF, CFR, EXW terms from Shanghai, Guangzhou, and Ningbo ports.
High Repeat Buyer Rate: 80% to 100% of customers are repeat buyers.
Comprehensive Product Range: Manufacturer of tablets, capsules, eye drops, injections, syrups, and creams.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs CertifiedExport Year: 21 Years CertifiedNearest Port: Shanghai Port, Guangzhou Port, Ningbo PortAverage Response Time: ≤24h
AI-Powered supplier vetting
SummaryJIANGXI XIERKANGTAI PHARMACEUTICAL CO., LTD. is a China-based manufacturing factory established in 2004, with 126 employees and a combined business entity structure. Its stated scope covers pharmaceutical dosage forms, raw-material production and processing, and exports. The supplier reports customization from samples and designs, documented finished-product inspection, complaint handling, traceability, and quality-assurance procedures. It offers OEM services to well-known brands and has six R&D engineers, but reports no new products during the past year, no ODM service, and no SDK. Export sales account for 90% of total sales, with one-month stated lead times in both peak and off-season periods. Certification details are listed only as “Others,” and no cooperation with Fortune 500 companies is reported. Financial credibility cannot be assessed because the provided information does not include non-financial financial evidence.
Supplier typeThe supplier is identified as a factory and limited company in China, established on January 16, 2004, with 126 employees. Its stated business scope includes pharmaceutical production, processing, and export of raw materials, indicating a manufacturing-oriented supplier rather than a purely trading entity.
After-Sales capabilityThe supplier reports documented and followed procedures for handling customer complaints, service-capability assessment, corrective and preventive actions, and supplier management. However, the stated overseas-service coverage is 0 countries, so the evidence supports internal service processes but not broad overseas after-sales reach.
R&D capabilityThe supplier has six R&D engineers and provides OEM services to well-known brands. However, it reports no new products in the past year, no ODM service, and no available SDK, indicating that documented innovation and independent product-development capability are limited.
Production capacityThe supplier lists multiple pharmaceutical and equipment-related production capabilities, has a stated pharmaceutical manufacturing and processing scope, and reports uniformly followed finished-product inspection instructions. It also reports one-month average lead times in both peak and off-season periods, supporting evidence of established production operations.
Customization capabilityThe supplier explicitly supports customization from samples and from customer designs, and also reports OEM capability for well-known brands. Although it does not provide ODM services, the evidence directly supports customer-led customization and OEM production.
Product Q&A
Q:Is this product GMP certified?
A:
Yes, it is produced in a GMP factory and certified by China GMP and more than ten countries' MOH.
Q:What is the dosage for Diclofenac Tablet 50mg?
A:
Oral administration is typically 1 time a day, or 1 or 2 times a day, or as directed by a doctor.
Q:What are the main indications for this tablet?
A:
It is used for acute and chronic rheumatoid arthritis, ankylosing spondylitis, osteoarthritis, and soft tissue injuries.
Q:Can I customize the product?
A:
Yes, OEM service is available with customization options from samples and designs.
Q:What are the common adverse reactions?
A:
Common reactions include headache, abdominal pain, gastrointestinal issues, and occasional dizziness.
Send Inquiry
*To:
JIANGXI XIERKANGTAI PHARMACEUTICAL CO., LTD.
JIANGXI XIERKANGTAI PHARMACEUTICAL CO., LTD.*Content:
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