Mefdel - P DS Susp is a pharmaceutical suspension formulated with Mefenemic 100mg and Paracetamol 250mg, designed for therapeutic use under medical supervision. The formulation ensures optimal solubility, stability, and uniform dispersion of active ingredients in a suspension medium. The combination of Mefenemic, a non-steroidal anti-inflammatory drug (NSAID), and Paracetamol, a centrally acting analgesic, is carefully balanced to achieve synergistic pharmacological effects. The suspension is prepared using advanced emulsification and homogenization techniques to ensure consistent particle size distribution, enhancing bioavailability and reducing sedimentation. The DPCO (Drug Price Control Order) compliance ensures cost-effective pricing while maintaining pharmaceutical quality. The formulation is designed for ease of administration, with a ready-to-use suspension that requires no further dilution, making it suitable for both institutional and retail settings.
Manufacturing Capability
Our manufacturing infrastructure is equipped with state-of-the-art facilities compliant with current Good Manufacturing Practices (cGMP) and ISO 9001 standards. The production of Mefdel - P DS Susp involves aseptic processing capabilities for suspension preparation, ensuring sterility and microbial safety. The facility is designed for scalable production, enabling efficient bulk supply to meet global demand. Advanced analytical instrumentation, including High-Performance Liquid Chromatography (HPLC) and Dissolution Testing Systems, ensures precise formulation control. The manufacturing process adheres to strict quality systems, including Hazard Analysis and Critical Control Points (HACCP), to mitigate risks and ensure product consistency. Our facility supports both small-scale prototyping and large-volume production, with dedicated lines for suspension manufacturing to maintain product integrity and compliance.
Available Strengths and Packaging
Composition: Mefenemic 100mg + Paracetamol 250mg Suspension (DPC, DPCO)
Packaging: 60ml With Outer
The product is available in a single strength of 100mg Mefenemic and 250mg Paracetamol per 60ml suspension, packaged in a 60ml container with an outer packaging layer for secure distribution. The formulation is designed for stability during storage and transportation, ensuring product integrity under standard pharmaceutical conditions.
Contract Manufacturing / Third Party Manufacturing
As a trusted pharmaceutical manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to meet the needs of global buyers. Our capabilities include private label manufacturing, where we produce under a client’s brand name, ensuring full customization of packaging, labeling, and formulation. We support contract manufacturing for both generic and branded formulations, adhering to regulatory standards and client specifications. Our facility is equipped to handle complex pharmaceutical requirements, including API integration, excipient compatibility testing, and final product packaging. For pharmaceutical buyers seeking scalable solutions, we provide end-to-end manufacturing support, from formulation development to bulk supply, ensuring compliance with global quality and regulatory frameworks.
Quality Assurance
Our quality assurance systems are designed to ensure consistency, safety, and efficacy in every batch of Mefdel - P DS Susp. Rigorous batch testing protocols include physicochemical analysis, microbial limit testing, and dissolution profiling to confirm product performance. Analytical validation is conducted using validated HPLC methods to quantify active ingredients and excipients, ensuring adherence to pharmacopeial standards. Quality control measures are integrated throughout the manufacturing process, with real-time monitoring of critical parameters such as pH, viscosity, and particle size. All products undergo final inspection and documentation to meet ISO 9001 and cGMP requirements, ensuring compliance with international pharmaceutical quality standards.
Regulatory Compliance
We maintain full compliance with Good Manufacturing Practices (GMP), World Health Organization (WHO) guidelines, and ISO 9001 standards to ensure product quality and safety. Our manufacturing processes adhere to global regulatory frameworks, including the U.S. FDA, EU GMP, and ICH guidelines, enabling seamless export to international markets. The product is formulated in accordance with DPCO regulations, ensuring affordability without compromising therapeutic efficacy. Our facility is regularly audited by regulatory authorities and third-party agencies to maintain compliance with evolving pharmaceutical standards. This commitment to regulatory adherence ensures that Mefdel - P DS Susp meets the stringent requirements of global buyers and healthcare systems.
Global Supply Capability
With a robust international distribution network, we provide reliable bulk supply to pharmaceutical buyers across multiple continents. Our export capabilities are supported by strategic logistics partnerships, ensuring timely delivery of products to destinations worldwide. The 60ml packaging is optimized for bulk supply, enabling efficient storage and transportation while maintaining product stability. Our supply chain is designed for reliability, with inventory management systems to meet urgent demand and ensure uninterrupted supply. We support both small and large-scale orders, offering flexible shipping options to accommodate diverse market needs.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners choose us for our expertise in high-quality pharmaceutical production, regulatory compliance, and global supply capabilities. Our commitment to cGMP standards, ISO certification, and DPCO compliance ensures that Mefdel - P DS Susp meets the demands of international markets. As a trusted manufacturer, we offer end-to-end solutions, from formulation to bulk supply, with a focus on scalability, cost-effectiveness, and compliance. Our dedicated customer support team provides tailored assistance, ensuring seamless collaboration and satisfaction for all partners.
Bulk Supply Inquiry
We offer competitive bulk supply options for Mefdel - P DS Susp. For inquiries regarding large-scale procurement, please contact our sales team at info@delwishealthcare.com.
FAQs
What manufacturing standards does Mefdel - P DS Susp adhere to?
Our product is manufactured in compliance with cGMP, ISO 9001, and WHO guidelines, ensuring adherence to global pharmaceutical quality standards.
Can the product be customized for private label manufacturing?
Yes, we offer private label manufacturing services, allowing clients to brand the product under their own name.
What is the shelf life of Mefdel - P DS Susp?
The product has a shelf life of 24 months when stored under recommended conditions (cool, dry, and protected from light).
Is the packaging suitable for bulk supply?
The 60ml packaging with outer layer is designed for efficient bulk supply, ensuring product integrity during transportation.
Does the formulation comply with DPCO regulations?
Yes, the product is formulated in accordance with DPCO guidelines to ensure affordability and accessibility.
What quality control measures are in place for batch testing?
Each batch undergoes rigorous testing, including HPLC analysis, microbial testing, and dissolution profiling, to ensure consistency and safety.
Can the product be exported to international markets?
Yes, our compliance with global regulatory frameworks enables seamless export to markets worldwide.
What is the minimum order quantity for bulk supply?
We accommodate both small and large orders, with flexible minimum quantities based on client requirements.
How does your supply chain ensure reliability?
Our logistics network and inventory management systems ensure timely delivery, with dedicated support for urgent orders.
Can you provide documentation for regulatory compliance?
Yes, we supply complete regulatory documentation, including GMP certificates, batch records, and compliance reports.
