Mefdel - P is a dual-action pharmaceutical formulation combining Mefenemic (250mg) and Paracetamol (325mg) in a compressed tablet form. The formulation is engineered to ensure optimal dissolution, bioavailability, and stability through advanced excipient selection and controlled-release technology. Mefenemic, a non-steroidal anti-inflammatory drug (NSAID), is combined with Paracetamol, a widely used analgesic and antipyretic, to provide synergistic pain relief and fever reduction. The tablet matrix is designed to maintain chemical stability under varying environmental conditions, with excipients such as microcrystalline cellulose, magnesium stearate, and colloidal silicon dioxide ensuring uniformity in tablet weight, hardness, and disintegration time. The formulation undergoes rigorous testing for physicochemical properties, including pH compatibility, moisture resistance, and tablet integrity, to meet international pharmaceutical standards.
Manufacturing Capability
Our state-of-the-art pharmaceutical manufacturing facility is equipped with advanced infrastructure to produce high-quality combination tablets like Mefdel - P. The facility adheres to Good Manufacturing Practices (GMP) and employs sterile processing capabilities for critical stages of production, ensuring contamination-free manufacturing. High-speed tabletting machines, automated packaging lines, and precision dosing systems enable consistent batch production while maintaining strict quality control. The manufacturing process includes continuous monitoring of critical parameters such as temperature, humidity, and particle size to ensure product consistency. Our production capacity is scalable to meet bulk supply demands, with flexible manufacturing lines capable of accommodating varying formulations and packaging formats. The facility is certified under ISO 9001 and ISO 14001 standards, reflecting our commitment to quality, safety, and environmental sustainability.
Available Strengths and Packaging
Composition: Mefenemic 250mg + Paracetamol 325mg Tab
Packaging: 10x10 Blister
Mefdel - P is available in a standardized dosage form of 250mg Mefenemic and 325mg Paracetamol, packaged in a 10x10 blister format. The blister packaging ensures product protection against moisture, light, and contamination, while its tamper-evident design enhances security and compliance with regulatory requirements. This packaging format is ideal for pharmaceutical suppliers seeking efficient storage, transportation, and retail display solutions.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to the needs of pharmaceutical buyers. Our private label manufacturing capabilities allow clients to produce branded formulations under their own brand names, with full customization of packaging, labeling, and dosage forms. We support both small-scale and large-volume production, enabling flexibility for global market demands. Our team of pharmacists and engineers ensures adherence to regulatory guidelines while optimizing formulation stability, cost-efficiency, and scalability. Whether you require API sourcing, formulation development, or full-scale production, we provide end-to-end solutions to streamline your supply chain and accelerate time-to-market.
Quality Assurance
Our quality assurance framework is built on rigorous testing, analytical validation, and compliance with global pharmaceutical standards. Every batch of Mefdel - P undergoes comprehensive quality control checks, including dissolution testing, hardness measurement, and disintegration time analysis to ensure uniform performance. Advanced analytical techniques such as High-Performance Liquid Chromatography (HPLC) and Ultraviolet-Visible (UV-Vis) spectroscopy are employed to validate active ingredient content and purity. Microbial contamination testing, heavy metal analysis, and stability studies are conducted to guarantee product safety and shelf life. All quality control procedures are documented to meet International Council for Harmonisation (ICH) guidelines and United States Pharmacopeia (USP) standards, ensuring regulatory compliance and customer confidence.
Regulatory Compliance
We maintain strict adherence to Good Manufacturing Practices (GMP), World Health Organization (WHO) guidelines, and ISO 9001/14001 certification standards to ensure regulatory compliance across global markets. Our manufacturing processes align with FDA, EMA, and PIC/S requirements, enabling seamless export to regions with stringent pharmaceutical regulations. All documentation, including batch records, stability data, and quality test reports, is prepared to support regulatory submissions and audits. We also comply with the International Pharmaceutical Excipients Council (IPEC) guidelines for excipient sourcing and handling, ensuring transparency and traceability throughout the supply chain. This commitment to compliance positions us as a reliable partner for pharmaceutical manufacturers seeking global market access.
Global Supply Capability
Our export capabilities are supported by an extensive international distribution network and robust supply chain infrastructure. We provide bulk supply options to meet the demands of pharmaceutical distributors, exporters, and contract manufacturers worldwide. With strategic partnerships in key markets, we ensure timely delivery of high-quality products while maintaining cost-efficiency and supply chain reliability. Our facility is equipped to handle large-scale production, with storage capacities and logistics systems designed for seamless bulk supply. We prioritize supply chain resilience through diversified shipping routes, real-time tracking systems, and compliance with international shipping regulations, ensuring uninterrupted delivery even in challenging market conditions.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners choose us for our expertise in high-quality formulation development, regulatory compliance, and scalable production. Our commitment to GMP standards, advanced manufacturing technology, and global market access ensures reliable supply chains and competitive product offerings. We offer tailored solutions to meet the unique needs of our clients, from private label manufacturing to bulk supply agreements. With a focus on innovation, sustainability, and customer satisfaction, we deliver value-driven partnerships that enhance your market presence and operational efficiency.
Bulk Supply Inquiry
For bulk supply inquiries, please contact our sales team at info@delwishealthcare.com. Our dedicated team is ready to assist with customized solutions, including bulk procurement, packaging specifications, and regulatory documentation to support your global distribution efforts.
FAQs
What manufacturing standards does Mefdel - P comply with?
Mefdel - P is manufactured in compliance with GMP, WHO, ISO 9001, and ISO 14001 standards, ensuring quality, safety, and environmental responsibility.
Can Mefdel - P be produced in different packaging formats?
Yes, we offer flexible packaging options, including blister packs, strips, and bottles, to meet diverse market requirements.
What is the shelf life of Mefdel - P?
The shelf life of Mefdel - P is typically 24 months when stored under recommended conditions, as confirmed by stability testing.
Does your facility support private label manufacturing?
Yes, we provide private label manufacturing services, allowing clients to brand products under their own name.
How do you ensure the quality of active ingredients?
We source APIs from certified suppliers and conduct rigorous testing for purity, potency, and consistency using HPLC and other analytical methods.
Can you supply Mefdel - P in bulk quantities?
Yes, our facility is equipped for bulk production, with scalable capabilities to meet large-scale distribution needs.
What regulatory documentation is provided with each batch?
Each batch includes complete documentation, including batch records, stability data, and quality test reports for regulatory compliance.
How do you handle export logistics?
We manage export logistics through a global distribution network, ensuring compliance with international shipping regulations and timely delivery.
What is the minimum order quantity for Mefdel - P?
Minimum order quantities are flexible and can be customized based on production capacity and client requirements.
How can I request a sample of Mefdel - P?
Samples can be requested by contacting our sales team at info@delwishealthcare.com, with details on availability and shipping options.
