Diclowis - P is a dual-action analgesic formulation combining Diclofenac Potassium (50mg) and Paracetamol (325mg) in a single tablet. The formulation leverages the anti-inflammatory and cyclooxygenase (COX) inhibiting properties of diclofenac with the rapid-acting analgesic effects of paracetamol, creating a synergistic therapeutic profile. The tablet is manufactured using advanced excipient blends, ensuring optimal disintegration, dissolution, and bioavailability. The formulation is designed to maintain chemical stability under standard storage conditions, with controlled release characteristics to ensure consistent therapeutic efficacy. The combination of active ingredients is carefully balanced to meet pharmacological requirements while minimizing potential interactions, making it a versatile option for pharmaceutical manufacturers. The tablet’s compact design and uniform coating enhance its usability in packaging and distribution, supporting efficient supply chain integration.
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 line includes high-speed tablet presses, automated coating systems, and advanced drying and packaging equipment, enabling precise control over tablet hardness, weight variation, and disintegration time. Sterile processing capabilities are available for critical components, ensuring contamination-free production. The facility adheres to rigorous quality control protocols, including real-time monitoring of critical parameters such as temperature, humidity, and particle size. Production scalability is achieved through modular design, allowing seamless expansion to meet bulk supply demands without compromising product integrity. Comprehensive quality systems, including traceability and documentation, ensure full compliance with regulatory requirements and support efficient batch tracking.
Available Strengths and Packaging
Composition: Diclofenac Potassium 50mg + Paracetamol 325 mg Tab
Packaging: 20x10 Blister
Diclowis - P is available in a standardized strength of 50mg Diclofenac Potassium combined with 325mg Paracetamol. The blister packaging (20x10) provides robust protection against moisture, light, and physical damage, ensuring product stability during storage and transportation. This packaging format is ideal for retail and hospital use, offering convenient access and enhanced shelf life. The design also supports efficient inventory management and compliance with pharmaceutical packaging regulations.
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 or generic versions of Diclowis - P, with full customization of packaging, labeling, and formulation specifications. We support scalable production runs, ensuring consistent quality and adherence to global regulatory standards. Our team collaborates closely with clients to optimize manufacturing processes, reduce time-to-market, and ensure compliance with local and international guidelines. Whether you require bulk supply or niche market-specific formulations, our flexible manufacturing solutions are designed to meet diverse business requirements.
Quality Assurance
Our quality assurance framework is built on rigorous analytical validation, batch testing, and adherence to pharmaceutical quality standards. Each 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 contamination. Raw materials are sourced from certified suppliers and subjected to stringent incoming inspection protocols. Process validation, stability testing, and in-process monitoring ensure consistent product quality. All quality control measures are documented to meet cGMP, ISO, and WHO requirements, providing pharmaceutical buyers with confidence in product reliability and compliance.
Regulatory Compliance
Diclowis - P is manufactured in full compliance with Good Manufacturing Practices (GMP), WHO guidelines, and ISO 9001:2015 standards. Our facility is regularly audited by regulatory bodies to ensure adherence to international quality benchmarks. The product meets specifications for active pharmaceutical ingredients (APIs), excipients, and packaging materials, ensuring compatibility with global regulatory frameworks. We maintain detailed documentation for regulatory submissions, including batch records, stability data, and analytical reports. Compliance with export regulations and labeling requirements ensures seamless market entry in regions with stringent pharmaceutical standards.
Global Supply Capability
We provide robust global supply capabilities, including bulk supply options and international distribution networks. Our export infrastructure supports seamless delivery to over 50 countries, with partnerships ensuring reliable logistics and customs compliance. Bulk supply capacity is optimized through automated production lines and efficient inventory management systems, enabling timely fulfillment of large orders. Our supply chain reliability is reinforced by redundant quality control checkpoints, real-time tracking systems, and contingency planning for disruptions. Whether you require localized distribution or cross-border exports, our infrastructure ensures consistent product availability and adherence to global supply chain standards.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our expertise in high-quality formulation, regulatory compliance, and scalable production. Our commitment to cGMP, ISO, and WHO standards ensures product reliability and market competitiveness. We offer tailored solutions, from private label manufacturing to bulk supply, with competitive pricing and flexible order volumes. Our dedicated customer support team provides end-to-end assistance, from regulatory consultations to logistics coordination. With a proven track record of meeting global demand, we are your trusted partner for reliable, compliant pharmaceutical manufacturing.
Bulk Supply Inquiry
For bulk supply inquiries, please contact us at info@delwishealthcare.com. Our team is ready to assist with customized solutions, including large-scale production, packaging specifications, and export logistics.
FAQs
What manufacturing standards does Diclowis - P comply with?
Diclowis - P is manufactured in full compliance with cGMP, WHO guidelines, and ISO 9001:2015 standards, ensuring adherence to global pharmaceutical quality benchmarks.
Can Diclowis - P be produced in different packaging formats?
While the standard packaging is 20x10 blister, we offer customization options for alternative packaging formats upon request, subject to regulatory approval and client specifications.
What is the shelf life of Diclowis - P?
The product has a shelf life of 24 months when stored under recommended conditions (cool, dry, and protected from light). Stability testing confirms its potency throughout this period.
Does your facility support sterile manufacturing processes?
Yes, our facility is equipped with sterile processing capabilities for critical components, ensuring contamination-free production of pharmaceutical products.
Can you provide bulk supply for international markets?
Absolutely. We specialize in bulk supply for global markets, with a robust export infrastructure and logistics network to ensure timely and compliant delivery.
What quality control measures are in place for Diclowis - P?
Each batch undergoes rigorous testing, including HPLC analysis, dissolution testing, and microbial limit checks, ensuring compliance with regulatory standards.
Are there options for private label manufacturing?
Yes, we offer private label manufacturing services, allowing clients to produce branded versions of Diclowis - P with customized packaging and labeling.
How do you ensure supply chain reliability?
Our supply chain is supported by real-time tracking systems, redundant quality control checkpoints, and contingency planning, ensuring consistent product availability and delivery.
Can you assist with regulatory submissions for export markets?
Yes, our team provides regulatory support, including documentation for cGMP, WHO, and local market requirements, to facilitate seamless product approval and distribution.
What is the minimum order quantity for bulk supply?
Minimum order quantities are flexible and tailored to client needs. For specific requirements, please contact our sales team at info@delwishealthcare.com.
