Paris 650 is a pharmaceutical formulation optimized for stability, bioavailability, and consistent therapeutic performance. The core component, paracetamol (650mg), is combined with excipients such as microcrystalline cellulose, croscarmellose sodium, and magnesium stearate to ensure uniformity in tablet weight, disintegration, and dissolution. The formulation is designed for direct compression, enabling efficient production while maintaining tablet integrity during storage and transportation. The excipient selection ensures compatibility with various manufacturing processes and minimizes the risk of degradation under standard storage conditions. The product’s pharmaceutical profile supports rapid absorption and sustained efficacy, making it suitable for bulk supply in diverse therapeutic applications.
Manufacturing Capability
Our manufacturing infrastructure is engineered to meet the stringent demands of pharmaceutical production, with a focus on scalability, sterility, and compliance. The facility is equipped with state-of-the-art tablet compression machines, automated blister packaging systems, and advanced quality control laboratories. Sterile processing capabilities are maintained through ISO 7洁净室 environments, ensuring contamination-free production for sensitive formulations. All manufacturing processes adhere to Good Manufacturing Practice (GMP) guidelines, with continuous monitoring of critical parameters such as tablet hardness, disintegration time, and content uniformity. The facility supports large-scale production, with the ability to scale up or down based on demand, while maintaining consistent product quality. Robust quality systems, including validated process controls and real-time data monitoring, ensure compliance with international pharmaceutical standards.
Available Strengths and Packaging
Composition: Paracetamol 650mg Tab.
Packaging: 10x15 Blister
Paris 650 is available in a single strength of 650mg paracetamol tablets, packaged in 10x15 blister packs. This packaging format ensures tamper-evidence, product protection, and efficient distribution, making it ideal for bulk supply in both domestic and international markets.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing and private label services tailored to pharmaceutical buyers’ needs. Our capabilities include formulation development, tablet compression, blister packaging, and full-scale production for third-party clients. We support customization of packaging formats, labeling, and dosage strengths, enabling clients to meet specific market requirements. Our private label manufacturing services allow brands to produce high-quality products under their own trademarks, with full traceability and compliance. Whether you require small batch trials or large-scale production, our flexible manufacturing solutions ensure timely delivery and adherence to global quality standards.
Quality Assurance
Our quality assurance framework is built on rigorous analytical validation, batch testing, and compliance with international pharmaceutical standards. Every production batch undergoes comprehensive testing, including high-performance liquid chromatography (HPLC) for active ingredient quantification, dissolution testing to ensure bioavailability, and microbial limit checks for sterility. Raw materials are sourced from certified suppliers and subjected to incoming quality checks, while in-process controls monitor critical parameters during manufacturing. Final product testing includes physical attributes such as tablet hardness, disintegration time, and content uniformity. All quality control procedures are validated and documented to meet ICH, USP, and EP guidelines, ensuring consistency and reliability for global distribution.
Regulatory Compliance
Paris 650 is manufactured in full compliance with Good Manufacturing Practice (GMP) standards, including FDA 21 CFR Part 210/211, EMA guidelines, and WHO recommendations. The product adheres to ISO 9001 quality management systems and ISO 14001 environmental management standards, ensuring sustainable and ethical production. Regulatory compliance extends to packaging materials, which meet FDA and EU regulations for pharmaceutical blister packs. Our facility is regularly audited by international regulatory bodies, and all documentation is prepared to meet the requirements of the US, EU, Japan, and other key markets. This ensures seamless approval processes for export and distribution across global pharmaceutical supply chains.
Global Supply Capability
With a robust international distribution network, we provide reliable bulk supply to over 50 countries, supported by a logistics infrastructure designed for efficiency and compliance. Our export capabilities include compliance with customs regulations, phytosanitary certificates, and documentation for global trade. Bulk supply capacity is scalable, with the ability to meet demand for both small and large orders through optimized inventory management and just-in-time production. Our supply chain reliability is reinforced by partnerships with certified freight forwarders and adherence to international shipping standards, ensuring timely delivery without compromising product integrity.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturers select us for our unwavering commitment to quality, compliance, and scalability. Our GMP-certified facility ensures consistent product standards, while our flexible manufacturing solutions cater to diverse market needs. As a trusted supplier, we offer competitive pricing, rapid turnaround times, and full transparency in production and quality control. Our expertise in regulatory compliance and global supply chain management enables seamless integration into international markets, making us an ideal partner for bulk supply and contract manufacturing.
Bulk Supply Inquiry
For bulk supply inquiries, please contact our team at info@delwishealthcare.com.
FAQs
What certifications does Paris 650 hold?
Paris 650 is manufactured in compliance with GMP, ISO 9001, and WHO guidelines, ensuring adherence to global pharmaceutical standards.
Can the packaging format be customized?
Yes, we offer customization of packaging formats, including blister packs, to meet specific market requirements.
What regulatory approvals are required for export?
Our product complies with FDA, EMA, and WHO regulations, ensuring smooth export approvals for international markets.
What is the minimum order quantity for bulk supply?
We accommodate orders of all sizes, with flexible production schedules to meet both small and large-scale demand.
How is quality controlled during manufacturing?
Every batch undergoes rigorous testing, including HPLC, dissolution, and microbial analysis, with full documentation for traceability.
Can Paris 650 be produced under private label?
Yes, our private label manufacturing services allow brands to produce high-quality products under their own trademarks.
What is the shelf life of Paris 650?
The product has a shelf life of 24 months when stored under recommended conditions, as validated by stability testing.
How long does it take to process a bulk order?
Lead times vary based on order size, but we prioritize efficient production to ensure timely delivery without compromising quality.
Are there options for customized labeling?
Yes, we support customized labeling and packaging to align with client branding and regulatory requirements.
What support is available for regulatory documentation?
Our team provides complete regulatory documentation, including batch certificates, stability reports, and compliance certificates for global markets.
