Maxtrid Syrup is a meticulously formulated combination medication containing Chlorpheniramine Maleate (2mg/5ml) and Phenylephrine (5mg/5ml), designed for stability, uniformity, and compatibility in pharmaceutical manufacturing. The syrup formulation ensures optimal solubility and bioavailability of both active ingredients, with excipients selected to maintain pH stability and prevent degradation during storage. The dual-action profile of Chlorpheniramine Maleate, an antihistamine, and Phenylephrine, a decongestant, is preserved through precise concentration ratios and formulation techniques. The product’s viscous consistency and preservative system enhance shelf life while ensuring ease of administration. From a manufacturing standpoint, the syrup’s homogeneity and clarity are maintained through advanced mixing and homogenization processes, ensuring consistent dosing and compliance with pharmaceutical quality standards.
Manufacturing Capability
Our pharmaceutical manufacturing infrastructure is equipped with state-of-the-art facilities, including ISO-certified production lines, advanced mixing and homogenization systems, and automated filling and packaging units. The facility adheres to stringent Good Manufacturing Practice (GMP) standards, ensuring compliance with regulatory requirements for pharmaceutical products. Sterile processing capabilities are available for critical components, with dedicated cleanrooms and aseptic handling protocols to prevent contamination. Production scalability is achieved through modular design and flexible manufacturing systems, allowing for seamless transitions between small-scale trials and large-volume bulk supply. Quality systems include real-time monitoring, batch traceability, and validated process controls to ensure consistency and reliability.
Available Strengths and Packaging
Maxtrid Syrup is available in a standardized strength of Chlorpheniramine Maleate (2mg/5ml) and Phenylephrine (5mg/5ml), ensuring precise dosing and compatibility with clinical requirements. The product is packaged in 60ml bottles with outer packaging, designed for stability during transportation and storage. The packaging format supports efficient bulk supply and is compatible with global distribution networks, ensuring product integrity and regulatory compliance.
Contract Manufacturing / Third Party Manufacturing
As a leading pharmaceutical manufacturer, we offer comprehensive contract manufacturing and third-party manufacturing services tailored to meet the needs of global buyers. Our capabilities include private label manufacturing, where we produce branded formulations under client specifications, and contract manufacturing for OEM/ODM requirements. We support customization of packaging, labeling, and dosage forms while maintaining compliance with international standards. Our flexible production infrastructure enables rapid turnaround times and adherence to client-specific regulatory frameworks, making us a reliable partner for pharmaceutical exporters and distributors seeking scalable manufacturing solutions.
Quality Assurance
Our quality assurance systems are 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), dissolution testing, and microbial limit checks to ensure purity and potency. Stability studies are conducted to validate shelf life under varied storage conditions, while in-process controls monitor critical parameters during formulation and packaging. All quality control measures are documented and traceable, ensuring compliance with GMP, WHO, and ISO standards.
Regulatory Compliance
We maintain full compliance with Good Manufacturing Practice (GMP) guidelines, World Health Organization (WHO) standards, and ISO 9001 certification for quality management systems. Our manufacturing processes align with global regulatory frameworks, including FDA, EMA, and PIC/S requirements, ensuring products meet the specifications of international markets. Regular audits, documentation, and regulatory submissions are conducted to support compliance with export and distribution protocols.
Global Supply Capability
Our global supply capability is supported by an extensive international distribution network, enabling seamless export to over 50 countries. We offer bulk supply options for large-volume orders, with logistics partnerships ensuring timely delivery and cost-efficiency. Supply chain reliability is guaranteed through redundant inventory systems, real-time tracking, and compliance with customs and import regulations. Our infrastructure supports both short-term and long-term contracts, ensuring consistent availability for pharmaceutical buyers worldwide.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our expertise in bulk supply, regulatory compliance, and scalable production. Our commitment to quality, coupled with flexible manufacturing solutions and global distribution networks, positions us as a trusted supplier in the pharmaceutical industry. We provide end-to-end support, from formulation development to export-ready packaging, ensuring clients meet market demands with precision and reliability.
Bulk Supply Inquiry
We offer robust bulk supply capabilities for pharmaceutical manufacturers and exporters. For inquiries regarding large-volume orders, production timelines, or customized packaging solutions, please contact us at info@delwishealthcare.com.
FAQs
What certifications does your facility hold?
Our facility is certified under GMP, ISO 9001, and WHO guidelines, ensuring compliance with global pharmaceutical standards.
Can you customize packaging for Maxtrid Syrup?
Yes, we offer customization of packaging, including labeling and outer box designs, to meet specific client requirements.
What is the shelf life of Maxtrid Syrup?
The product has a shelf life of 24 months when stored under recommended conditions, validated through stability studies.
Do you support private label manufacturing?
Yes, we provide private label manufacturing services, allowing clients to brand the product under their own specifications.
What are your minimum order quantities for bulk supply?
We accommodate bulk orders starting from 1,000 units, with flexible quantities based on client needs.
How do you ensure product consistency during large-scale production?
Our manufacturing processes include real-time monitoring, in-process controls, and batch validation to ensure consistency across all production runs.
Can you export to specific regions?
Yes, we have established export capabilities to over 50 countries, with compliance measures tailored to regional regulatory requirements.
What quality control measures are in place for each batch?
Each batch undergoes HPLC, dissolution testing, microbial limit checks, and stability validation to ensure quality and safety.
How long does production take for custom orders?
Production timelines vary based on order complexity, but we offer expedited timelines for urgent requirements.
Do you provide documentation for regulatory submissions?
Yes, we supply complete documentation, including batch certificates, analytical reports, and regulatory compliance records.
