Uridel Syrup is a meticulously formulated oral liquid designed for pharmaceutical applications, combining Potassium Citrate 1100mg and Citric Acid Monohydrate 334mg in a flavoured Sorbitol Base (Alkaliser) to achieve precise pH and electrolyte balance. The formulation leverages the buffering capacity of Potassium Citrate to neutralize excess acidity, while Citric Acid Monohydrate provides controlled acidity, ensuring stability and compatibility with other pharmaceutical ingredients. The Sorbitol Base serves as a sugar-free, non-caloric excipient, enhancing palatability without compromising the product’s therapeutic profile. The syrup’s pH-adjusting properties make it suitable for use in pharmaceutical settings requiring controlled alkalization, such as intravenous solutions or electrolyte replenishment formulations. The formulation is designed for stability under standard storage conditions and compatibility with a wide range of pharmaceutical excipients, ensuring seamless integration into complex drug delivery systems.
Manufacturing Capability
Our pharmaceutical manufacturing infrastructure is equipped to produce Uridel Syrup at scale, adhering to stringent GMP standards and ensuring consistent quality. The facility features advanced sterile processing capabilities for oral liquid formulations, including closed-system filling and sealing to prevent contamination. Production scalability is achieved through modular manufacturing lines that support both small-batch and bulk production, accommodating varying demand without compromising quality. The facility maintains comprehensive quality systems, including validated cleaning protocols, environmental monitoring, and real-time data collection to ensure compliance with regulatory requirements. All manufacturing processes are designed to meet international standards, with dedicated areas for formulation development, blending, and packaging to prevent cross-contamination.
Available Strengths and Packaging
Uridel Syrup is available in a standardized strength of Potassium Citrate 1100mg + Citric Acid Monohydrate 334mg, formulated into a sugar-free, flavoured Sorbitol Base Syrup. The product is packaged in 100 ml single-dose containers, ensuring precise dosing and ease of integration into pharmaceutical supply chains.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer end-to-end contract manufacturing services for pharmaceutical buyers, including private label and custom formulation development. Our facility is equipped to handle third-party manufacturing requests, enabling partners to leverage our expertise in formulation science, GMP-compliant production, and regulatory compliance. We support the production of Uridel Syrup and similar alkalizing syrups for global markets, with the flexibility to adjust specifications, packaging, and production volumes to meet client requirements. Our team collaborates closely with clients to ensure alignment with their quality standards, regulatory needs, and market-specific demands.
Quality Assurance
Our quality assurance framework ensures rigorous control over every stage of Uridel Syrup production. Each batch undergoes comprehensive testing, including in-process analytical validation, pH profiling, and dissolution testing to confirm formulation integrity. Advanced analytical techniques such as HPLC and titration are employed to verify active ingredient content and purity. Stability studies are conducted to assess shelf life under accelerated conditions, ensuring compliance with pharmacopeial standards. All quality control measures are documented to meet GMP requirements, with traceability systems in place to support regulatory audits and supply chain transparency.
Regulatory Compliance
Uridel Syrup is manufactured in full compliance with GMP, WHO guidelines, and ISO 9001:2015 standards. Our facility holds certifications for Good Manufacturing Practices (GMP) and adheres to international regulatory frameworks, including FDA, EMA, and PIC/S guidelines. The product is formulated to meet pharmacopeial standards (USP, EP, BP) and is suitable for export to global markets. Our quality systems ensure compliance with regulatory inspections, with documented processes for change control, deviation management, and corrective action plans.
Global Supply Capability
With a robust international distribution network, we provide reliable bulk supply capabilities for Uridel Syrup, supporting exporters and distributors across multiple regions. Our logistics partners enable seamless cross-border shipments, ensuring timely delivery while maintaining product integrity. The 100 ml packaging is optimized for bulk supply, with scalable production to meet large-scale demand. Our supply chain is designed for resilience, incorporating contingency planning and real-time tracking to minimize disruptions. We offer customized export solutions, including compliance documentation and regulatory support for international markets.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our expertise in alkalizing syrup production, regulatory compliance, and scalable manufacturing. Our facility’s GMP-certified infrastructure, combined with a focus on quality and innovation, ensures reliable supply chains and product consistency. We provide tailored solutions for bulk supply, with the flexibility to adapt to evolving market demands. Our commitment to transparency, compliance, and customer collaboration positions us as a preferred partner for global pharmaceutical buyers.
Bulk Supply Inquiry
For bulk supply inquiries or to discuss customization options for Uridel Syrup, contact our team at info@delwishealthcare.com.
FAQs
What certifications does your facility hold for manufacturing Uridel Syrup?
Our facility is certified under GMP, ISO 9001:2015, and complies with WHO and FDA guidelines, ensuring adherence to global pharmaceutical standards.
Can Uridel Syrup be customized for different packaging sizes?
Yes, we offer flexible packaging options, including the standard 100 ml size, to meet specific market requirements.
What quality control measures are in place for Uridel Syrup?
Each batch undergoes rigorous testing, including HPLC, pH profiling, and stability studies, to ensure compliance with pharmacopeial standards.
Is Uridel Syrup suitable for export to international markets?
Yes, the formulation meets regulatory requirements for export, with documentation supporting compliance with FDA, EMA, and PIC/S guidelines.
Can you accommodate private label manufacturing for Uridel Syrup?
Absolutely. We provide private label manufacturing services, allowing clients to brand the product under their own specifications.
What is the minimum order quantity for bulk supply?
We support flexible bulk orders, with production capabilities tailored to meet both small and large-scale demands.
How do you ensure supply chain reliability for Uridel Syrup?
Our logistics network and real-time tracking systems ensure timely delivery, with contingency plans to mitigate supply chain disruptions.
What regulatory approvals are required for exporting Uridel Syrup?
We provide all necessary documentation, including Certificates of Analysis (CoA) and compliance reports, to meet international regulatory requirements.
Can Uridel Syrup be produced in different strengths?
While the standard strength is Potassium Citrate 1100mg + Citric Acid Monohydrate 334mg, we can customize formulations upon request.
How do you handle deviations during manufacturing?
Our quality management system includes robust deviation management protocols, with root cause analysis and corrective actions to ensure product consistency.
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