Delcold Plus Susp is a multi-ingredient suspension designed for pharmaceutical applications, combining Anti Cold C.P.Maleate, Paracetamol, and Phenylephrin HCl in a stable, homogeneous formulation. The suspension ensures uniform drug dispersion, enhancing bioavailability and ease of dosing. The formulation leverages advanced excipient compatibility testing to ensure stability under varied storage conditions. The active pharmaceutical ingredients (APIs) are carefully selected for their synergistic effects in addressing cold symptoms, while the suspension base provides a convenient delivery system for pharmaceutical manufacturers. The product’s formulation is optimized for scalability, with a focus on maintaining API integrity during mixing and homogenization processes. The suspension’s physical and chemical properties are validated through rigorous physicochemical testing to ensure consistency in manufacturing.
Manufacturing Capability
Delwis Healthcare’s manufacturing infrastructure is equipped with state-of-the-art facilities designed to meet the demands of pharmaceutical production. The facility includes a dedicated suspension formulation line with advanced mixing and homogenization equipment to ensure uniform dispersion of active ingredients. Sterile processing capabilities are maintained through ISO-certified cleanrooms, ensuring compliance with cGMP standards for pharmaceutical manufacturing. The production process adheres to strict quality control protocols, including real-time monitoring of temperature, pH, and viscosity parameters. Scalability is achieved through modular production lines capable of handling bulk orders without compromising product consistency. The facility’s quality systems are aligned with international standards, including ISO 9001 and 14001, ensuring environmental and operational excellence.
Available Strengths and Packaging
Composition: Anti Cold C.P.Maleate 2mg + Paracetamol 250 mg + Phenylephrin HCl 5mg Susp
Packaging: 60ml With Outer
Delcold Plus Susp is available in a 60ml single-dose suspension format, packaged in a robust outer container to ensure product integrity during transportation and storage. The suspension formulation is designed for easy dispensing and accurate dosing, making it suitable for both domestic and international markets. The packaging ensures compliance with regulatory requirements for pharmaceutical products, including child-resistant closures and tamper-evident seals.
Contract Manufacturing / Third Party Manufacturing
Delwis Healthcare offers comprehensive contract manufacturing and third-party manufacturing services tailored to pharmaceutical buyers’ needs. Our private label manufacturing capabilities allow clients to produce branded products under their own brand name, with full control over formulation, packaging, and labeling. We provide end-to-end solutions, from API sourcing to finished product packaging, ensuring compliance with global regulatory standards. Our contract manufacturing services are scalable, enabling clients to meet fluctuating demand without compromising quality. The facility’s flexibility supports customization of dosage forms, strengths, and packaging formats, making it an ideal partner for pharmaceutical manufacturers seeking to expand their product portfolios.
Quality Assurance
Quality assurance at Delwis Healthcare is rooted in rigorous analytical validation and adherence to pharmaceutical quality standards. Every batch undergoes comprehensive testing, including dissolution testing, microbial limit checks, and stability studies to ensure product consistency. Advanced analytical techniques such as HPLC and UV spectroscopy are employed for API quantification and impurity detection. Batch testing is conducted in accordance with ICH and USP guidelines, ensuring compliance with global quality benchmarks. Documentation is maintained in line with cGMP requirements, providing traceability and transparency throughout the supply chain.
Regulatory Compliance
Delwis Healthcare ensures full compliance with GMP, WHO guidelines, and ISO standards to meet the demands of global pharmaceutical markets. Our manufacturing processes adhere to ICH Q7 and USP <1210> guidelines for active pharmaceutical ingredients and finished dosage forms. The facility is certified under ISO 9001 for quality management and ISO 14001 for environmental management, reflecting our commitment to sustainable practices. Compliance with WHO prequalification standards enables export to developing markets, while adherence to FDA and EMA guidelines ensures access to mature pharmaceutical markets. All documentation is prepared to meet regulatory requirements for registration, import, and distribution.
Global Supply Capability
Delwis Healthcare is a trusted exporter with a robust international distribution network spanning over 50 countries. Our bulk supply capacity is supported by a logistics infrastructure designed for seamless global delivery, including temperature-controlled shipping and real-time tracking systems. The facility’s production capabilities ensure consistent supply to meet large-scale demand, with inventory management systems to mitigate supply chain disruptions. Export compliance is ensured through rigorous documentation, including COA, batch certificates, and regulatory approvals for target markets. Our supply chain reliability is further enhanced by partnerships with global logistics providers, ensuring timely delivery of pharmaceutical products to distributors and retailers.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners choose Delwis Healthcare for our unwavering commitment to quality, compliance, and scalability. Our expertise in multi-ingredient suspension manufacturing ensures consistent product performance, while our global supply network enables seamless market access. As a trusted manufacturer and supplier, we offer competitive pricing without compromising on regulatory standards. Our ability to deliver bulk supplies with short lead times makes us an ideal partner for businesses seeking reliable, high-quality pharmaceutical solutions.
Bulk Supply Inquiry
Delwis Healthcare offers bulk supply capabilities for Delcold Plus Susp. For inquiries regarding large-scale orders, please contact us at info@delwishealthcare.com.
FAQs
What manufacturing standards does Delwis Healthcare follow for Delcold Plus Susp?
Delwis Healthcare adheres to cGMP, WHO, ISO 9001, and ISO 14001 standards to ensure product quality and environmental compliance.
Can Delcold Plus Susp be customized for different packaging formats?
Yes, our facility supports customization of packaging formats, including 60ml suspension bottles with outer packaging.
What regulatory approvals are required for exporting Delcold Plus Susp?
Export compliance includes WHO prequalification, FDA, EMA, and regional regulatory approvals, ensuring global market access.
How does Delwis Healthcare ensure the stability of the suspension formulation?
Stability is ensured through rigorous physicochemical testing, including pH, viscosity, and microbial limit checks.
What is the minimum order quantity for bulk supply?
Bulk supply options are flexible, with quantities tailored to meet client requirements. Contact us for details.
Can Delwis Healthcare provide private label manufacturing for Delcold Plus Susp?
Yes, we offer private label manufacturing services, allowing clients to brand the product under their own name.
What quality control measures are in place for batch testing?
Every batch undergoes dissolution testing, microbial analysis, and API quantification using HPLC and UV spectroscopy.
How does Delwis Healthcare support supply chain reliability?
Our logistics network includes temperature-controlled shipping, real-time tracking, and partnerships with global carriers for timely delivery.
Are there options for contract manufacturing beyond Delcold Plus Susp?
Yes, we provide contract manufacturing services for a wide range of pharmaceutical products, including suspensions and tablets.
What certifications does Delwis Healthcare hold for pharmaceutical manufacturing?
Delwis Healthcare is certified under ISO 9001, ISO 14001, and complies with ICH and USP guidelines for pharmaceutical production.
