Zymed Tab is a multi-component tablet formulated to deliver a balanced therapeutic profile through its combination of Pancreatin, Simethicone, and Activated Charcoal. The formulation integrates Pancreatin, a pancreatic enzyme complex containing lipase, protease, and amylase, to aid in the breakdown of dietary fats, proteins, and carbohydrates. Simethicone, a surface-active agent, is incorporated to neutralize gas bubbles in the gastrointestinal tract, reducing bloating and discomfort. Activated Charcoal, a highly porous adsorbent, is included to bind excess gas and toxins, enhancing the tablet’s overall efficacy. The tablet’s design ensures uniform dispersion of active ingredients, with excipients selected for compatibility, stability, and disintegration properties. Manufacturing processes prioritize controlled particle size distribution, compression force optimization, and dissolution rate consistency to ensure uniform bioavailability. The formulation is designed to maintain stability under standard storage conditions, with rigorous testing for disintegration time, dissolution efficiency, and physicochemical compatibility of components.
Manufacturing Capability
Our pharmaceutical manufacturing infrastructure is equipped with state-of-the-art facilities compliant with global Good Manufacturing Practice (GMP) standards. The production process for Zymed Tab utilizes high-speed tablet presses and advanced blending systems to ensure homogenous distribution of active pharmaceutical ingredients (APIs). Sterile processing capabilities are maintained through ISO Class 7 cleanroom environments, ensuring contamination-free manufacturing. The facility adheres to strict GMP guidelines, with continuous monitoring of critical parameters such as temperature, humidity, and particle count. Production scalability is achieved through modular manufacturing lines capable of handling bulk orders while maintaining quality consistency. Quality systems include real-time process analytical technology (PAT) and automated data collection to ensure traceability and compliance. The facility is certified for ISO 9001 quality management and ISO 14001 environmental management, reflecting a commitment to sustainable and efficient manufacturing.
Available Strengths and Packaging
Composition: Pancreatin 175 mg + Simethicone 50 mg + Activated Charcoal 50 mg Tablet
Packaging: 10x10 Strip
Zymed Tab is available in a single strength formulation, with each tablet containing 175 mg of Pancreatin, 50 mg of Simethicone, and 50 mg of Activated Charcoal. The 10x10 strip packaging ensures convenient storage and distribution, with tamper-evident seals and child-resistant packaging options available upon request.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to pharmaceutical buyers. Our capabilities include private label manufacturing, where we produce Zymed Tab under a client’s brand name, ensuring full customization of packaging, labeling, and formulation specifications. Contract manufacturing partners benefit from our expertise in API sourcing, formulation development, and regulatory compliance, enabling seamless integration into global supply chains. We support clients in navigating complex regulatory landscapes by providing documentation for GMP, WHO, and ISO standards. Additionally, our flexible production model accommodates both small-scale trials and large-volume bulk orders, with dedicated teams to manage quality control, batch validation, and supply chain coordination.
Quality Assurance
Our quality assurance framework is built on rigorous analytical validation, batch testing, and adherence to international pharmaceutical standards. Each production batch undergoes comprehensive testing for potency, purity, and dissolution rate using high-performance liquid chromatography (HPLC) and Fourier-transform infrared spectroscopy (FTIR). Quality control systems include in-process testing for tablet hardness, disintegration time, and weight uniformity, ensuring compliance with pharmacopeial requirements. Batch validation is conducted in accordance with USP and EP guidelines, with documentation traceable to regulatory authorities. We maintain a robust quality management system (QMS) that integrates real-time monitoring, corrective and preventive actions (CAPA), and continuous improvement initiatives. All products are tested for microbial contamination, heavy metals, and residual solvents, ensuring safety and efficacy for global markets.
Regulatory Compliance
Zymed Tab is manufactured in full compliance with Good Manufacturing Practice (GMP) standards, including those set by the World Health Organization (WHO), the U.S. Food and Drug Administration (FDA), and the European Medicines Agency (EMA). Our facility holds certifications for ISO 9001:2015 quality management and ISO 14001:2015 environmental management, ensuring adherence to global regulatory frameworks. The product is formulated to meet pharmacopeial standards, with documentation available for regulatory submissions in major markets. We maintain compliance with the International Council for Harmonisation (ICH) guidelines, ensuring consistency in quality, safety, and efficacy across international borders. Regular audits by third-party regulatory bodies and internal quality reviews ensure ongoing compliance with evolving pharmaceutical regulations.
Global Supply Capability
Our global supply capability is supported by an extensive international distribution network and robust logistics infrastructure. We offer bulk supply options to meet the demands of pharmaceutical distributors, exporters, and contract manufacturers, with capacity to scale production based on market requirements. Export capabilities are enhanced by compliance with international shipping regulations, including IATA and IMDG standards for hazardous materials. Our supply chain ensures timely delivery through partnerships with trusted logistics providers, with real-time tracking and inventory management systems to guarantee reliability. Bulk supply capacity is supported by dedicated storage facilities and packaging lines, enabling efficient handling of large orders. We prioritize supply chain resilience through diversified sourcing, redundant production lines, and contingency planning to mitigate disruptions.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners choose us for our unwavering commitment to quality, compliance, and scalability. Our expertise in multi-component tablet formulation, combined with state-of-the-art manufacturing infrastructure, ensures consistent product performance. As a certified GMP supplier, we provide end-to-end solutions, from API sourcing to global distribution, reducing time-to-market for clients. Our ability to meet stringent regulatory requirements across multiple regions enables seamless entry into international markets. Additionally, our flexible production model and dedicated customer support ensure tailored solutions that align with the unique needs of each partner.
Bulk Supply Inquiry
For bulk supply inquiries, please contact us at info@delwishealthcare.com. Our team is ready to assist with order placement, customization, and logistics coordination to meet your pharmaceutical needs.
FAQs
What is the minimum order quantity for Zymed Tab bulk supply?
Our minimum order quantity is 10,000 tablets, with flexible options for smaller trials or larger-scale production.
Can Zymed Tab be customized for private label manufacturing?
Yes, we offer private label manufacturing services, allowing clients to brand Zymed Tab under their own label.
What certifications does your facility hold for pharmaceutical manufacturing?
Our facility is certified for ISO 9001:2015, ISO 14001:2015, and GMP compliance with WHO, FDA, and EMA standards.
How do you ensure the stability of Zymed Tab under storage conditions?
Stability is ensured through rigorous testing for moisture, temperature, and light sensitivity, with packaging designed to maintain product integrity.
What regulatory documentation is provided for export compliance?
We provide complete documentation for GMP, WHO, FDA, and EMA compliance, including batch certificates and regulatory submissions.
Can you accommodate special packaging requirements?
Yes, we offer customized packaging solutions, including child-resistant blister packs and tamper-evident seals.
What is the typical lead time for bulk orders?
Lead times vary based on order size, but we typically deliver within 4–6 weeks for standard bulk orders.
How do you handle quality control for each production batch?
Each batch undergoes HPLC, FTIR, and dissolution testing, with full documentation traceable to regulatory standards.
Are there options for API sourcing and formulation adjustments?
Yes, we provide API sourcing flexibility and can adjust formulations to meet specific client requirements.
What support is available for international shipping and customs compliance?
Our team assists with customs documentation, hazardous material compliance, and logistics coordination for global shipments.
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