Cilnidet T 10/40 is a fixed-dose combination tablet designed for pharmaceutical precision, combining Cilnidipine (a dihydropyridine calcium channel blocker) and Telmisartan (an angiotensin II receptor blocker). The formulation ensures compatibility between active ingredients, with excipients selected to maintain stability, uniformity, and disintegration properties. The tablet’s design incorporates a robust binding agent to prevent segregation of components during manufacturing, ensuring consistent release profiles. The formulation adheres to strict pharmaceutical standards, with controlled particle size distribution and flow characteristics to facilitate efficient compression. The final product exhibits a hardness of 50–60 Pascals, a disintegration time of ≤30 minutes, and a dissolution rate meeting ICH guidelines. The combination of these two pharmacologically distinct agents is optimized for sustained therapeutic action, with the formulation engineered to minimize potential interactions while maximizing bioavailability.
Manufacturing Capability
Our manufacturing infrastructure is equipped with state-of-the-art facilities compliant with current Good Manufacturing Practices (cGMP) and ISO 9001:2015 standards. The production line includes high-speed tablet presses, automated blending systems, and advanced coating equipment to ensure precision in tablet formation. Sterile processing capabilities are available for critical components, supported by ISO Class 7 cleanrooms and validated HVAC systems. The facility adheres to rigorous quality control protocols, including real-time monitoring of critical parameters such as moisture content, tablet weight variation, and dissolution testing. Scalability is ensured through modular production lines capable of handling bulk supply demands without compromising quality. Comprehensive quality systems, including traceability and change control, guarantee consistency across batches.
Available Strengths and Packaging
Composition: Cilnidipine 10mg + Telmisartan 40mg Tablets
Packaging: 10x10 Alu Alu
The product is available in a 10x10 Alu Alu blister pack, designed for secure storage and transport. The aluminum blister format provides moisture and light protection, ensuring product integrity during distribution. This packaging is ideal for pharmaceutical suppliers requiring reliable, tamper-evident packaging for global markets.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer contract manufacturing, private label production, and third-party manufacturing services tailored to pharmaceutical buyers. Our capabilities include formulation development, API integration, and finished dosage form production, with flexibility to meet specific regulatory and quality requirements. We support both domestic and international clients by adhering to global standards such as GMP, WHO, and FDA guidelines. Our team provides end-to-end solutions, from raw material sourcing to packaging, ensuring compliance with client specifications. Private label manufacturing is facilitated through customizable branding and packaging options, enabling clients to meet market-specific demands.
Quality Assurance
Our quality assurance framework is built on rigorous analytical validation, batch testing, and adherence to international standards. Each batch undergoes comprehensive testing, including High-Performance Liquid Chromatography (HPLC) for active ingredient quantification, dissolution testing, and microbial limit analysis. Process validation ensures consistency in tablet hardness, disintegration, and content uniformity. Quality control systems are integrated with advanced data analytics to detect deviations early, with corrective actions implemented through root-cause analysis. Compliance with ICH, USP, and EP monographs ensures product reliability for global markets.
Regulatory Compliance
We maintain full compliance with GMP, WHO guidelines, and ISO standards, including ISO 9001:2015 and ISO 14001 for environmental management. Our facility is audited regularly by regulatory bodies and third-party inspectors to ensure adherence to global frameworks such as FDA, EMA, and PIC/S. Documentation for regulatory submissions, including batch records, stability data, and method validation reports, is maintained to support audits and market approvals. Compliance with the WHO Prequalification Programme ensures our products meet international quality benchmarks for export.
Global Supply Capability
Our export capabilities span over 150 countries, supported by a robust international distribution network and logistics partnerships. Bulk supply capacity is optimized for large-scale pharmaceutical buyers, with flexible order quantities and timely delivery schedules. The supply chain is designed for redundancy, ensuring uninterrupted service even during unforeseen disruptions. We provide end-to-end logistics solutions, including customs documentation, temperature-controlled shipping, and real-time tracking, to meet the demands of global distributors and exporters.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our expertise in scalable production, regulatory compliance, and global supply chain reliability. Our commitment to quality, combined with competitive pricing and rapid turnaround times, positions us as a preferred partner for bulk supply needs. With a proven track record in manufacturing complex combination products, we deliver consistent, high-quality solutions tailored to meet the evolving demands of the pharmaceutical industry.
Bulk Supply Inquiry
We offer reliable bulk supply capabilities for Cilnidet T 10/40. For inquiries, contact our team at info@delwishealthcare.com.
FAQs
What manufacturing standards does Cilnidet T 10/40 comply with?
Our product adheres to GMP, WHO, and ISO 9001:2015 standards, ensuring compliance with global regulatory frameworks.
Can Cilnidet T 10/40 be customized for private label manufacturing?
Yes, we support private label manufacturing with customizable branding and packaging options.
What is the shelf life of Cilnidet T 10/40 in its packaging?
The 10x10 Alu Alu blister pack ensures a shelf life of 24 months under recommended storage conditions.
Does your facility support sterile manufacturing processes?
Yes, our ISO Class 7 cleanrooms are equipped for sterile processing of critical components.
What quality control tests are performed on each batch?
Each batch undergoes HPLC analysis, dissolution testing, and microbial limit checks to ensure product integrity.
Can you accommodate large-scale bulk orders?
Yes, our scalable production infrastructure supports bulk supply for global pharmaceutical buyers.
What regulatory certifications does your facility hold?
Our facility is certified under GMP, ISO 9001:2015, and WHO Prequalification Programme standards.
How do you ensure supply chain reliability?
We maintain redundant logistics networks and real-time tracking systems to ensure timely and consistent deliveries.
Are there options for alternative packaging formats?
While the standard packaging is 10x10 Alu Alu, we can accommodate custom packaging requests upon consultation.
How can I request a sample or bulk supply?
Contact our team at info@delwishealthcare.com for sample requests or to discuss bulk supply terms.
