Fernish Total is a precision-formulated multivitamin tablet designed for pharmaceutical manufacturers requiring a stable, high-purity combination of essential micronutrients. The formulation integrates Ferrous Ascorbate (100mg), a bioavailable iron source, with Methylcobalamin (1500mcg), a methylated form of vitamin B12, Folic Acid (1.5mg), and Zinc (22.5mg). These components are selected for their solubility, stability, and compatibility in a solid dosage form. The tablet’s formulation ensures uniform distribution of active ingredients, with excipients chosen to maintain tablet integrity, prevent degradation, and enhance disintegration properties. The combination of these micronutrients supports the development of products targeting anemia, metabolic support, and nutritional supplementation, aligning with global pharmaceutical trends toward comprehensive nutrient delivery.
Manufacturing Capability
Our manufacturing infrastructure is engineered to meet the stringent demands of pharmaceutical production, with state-of-the-art facilities equipped for large-scale tablet manufacturing. The facility includes a dedicated tablet compression line capable of producing high-volume batches while maintaining precise control over critical quality attributes such as tablet hardness, disintegration time, and content uniformity. Sterile processing capabilities are available for sensitive formulations, ensuring compliance with cGMP standards. The production process adheres to ISO 9001 and ICH guidelines, with continuous monitoring of parameters such as temperature, humidity, and particle size to ensure consistency. Scalability is a core strength, enabling seamless transitions from pilot batches to commercial production. Quality systems include validated analytical methods, automated data collection, and real-time process monitoring to guarantee reproducibility and regulatory compliance.
Available Strengths and Packaging
Fernish Total is available in a single strength: Ferrous Ascorbate 100mg + Methylcobalamin 1500mcg + Folic Acid 1.5mg + Zinc 22.5mg per tablet. The product is packaged in 10x10 Alu Alu blister packs, ensuring tamper-evidence, moisture resistance, and optimal shelf life. The aluminum blister packaging is designed for efficient storage, transportation, and retail display, with customization options for branding and labeling.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to pharmaceutical buyers’ needs. Our private label manufacturing capabilities allow clients to produce branded products under their own specifications, with full transparency in formulation, packaging, and quality control. We support both domestic and international clients by providing end-to-end solutions, from raw material sourcing to finished product delivery. Our team collaborates closely with buyers to align production processes with regulatory requirements, ensuring compliance with local and global standards. This flexibility enables pharmaceutical companies to leverage our expertise while maintaining brand autonomy and market competitiveness.
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 active ingredient content, dissolution profiles, microbial limits, and physical properties such as tablet weight and disintegration time. Advanced analytical techniques, including HPLC and ICP-MS, are employed to ensure accuracy and reproducibility. Quality control systems are integrated with validated process analytical technology (PAT) to enable real-time monitoring and corrective actions. All testing procedures comply with USP, EP, and ICH guidelines, ensuring consistency across batches and regulatory compliance.
Regulatory Compliance
Fernish Total is manufactured in full compliance with cGMP, WHO guidelines, and ISO 9001:2015 standards. Our facility is audited regularly by regulatory bodies and third-party inspectors to ensure adherence to global quality frameworks. The product meets specifications for both domestic and international markets, including the FDA, EMA, and PIC/S guidelines. Documentation is maintained in accordance with 21 CFR Part 11 for electronic records, and all manufacturing processes are validated to ensure reproducibility and traceability. This commitment to regulatory excellence positions Fernish Total as a reliable choice for pharmaceutical buyers seeking compliance with diverse market requirements.
Global Supply Capability
We offer robust global supply capabilities, with a well-established international distribution network spanning key markets in Asia, Europe, and the Americas. Our bulk supply capacity is designed to meet large-scale demand, with logistics infrastructure supporting timely delivery of finished products. The supply chain is optimized for reliability, featuring redundant inventory management, real-time tracking systems, and partnerships with trusted freight forwarders. Export capabilities are supported by compliance with international shipping regulations, including HS code classification and documentation for customs clearance. This ensures seamless global distribution while maintaining product integrity and regulatory compliance.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners select us for our unwavering commitment to quality, scalability, and regulatory compliance. Our expertise in multivitamin formulation, combined with advanced manufacturing capabilities, enables the production of high-standard products that meet global market demands. We offer competitive pricing without compromising on quality, supported by a dedicated account management team to address client needs promptly. Our ability to deliver bulk supply with consistent quality and timely delivery makes us a strategic partner for businesses seeking reliable, compliant pharmaceutical solutions.
Bulk Supply Inquiry
For bulk supply inquiries, please contact us at info@delwishealthcare.com. Our team is ready to assist with customized solutions, including packaging specifications, regulatory documentation, and production timelines.
FAQs
What manufacturing standards does Fernish Total comply with?
Fernish Total is manufactured in compliance with cGMP, WHO guidelines, and ISO 9001:2015 standards, ensuring adherence to global regulatory requirements.
Can Fernish Total be produced in different packaging formats?
While the standard packaging is 10x10 Alu Alu, we offer customization options for alternative packaging formats upon client request.
What is the shelf life of Fernish Total?
The product has a shelf life of 24 months when stored in optimal conditions (temperature ≤30°C, humidity ≤60%).
Is third-party manufacturing available for Fernish Total?
Yes, we provide third-party manufacturing services, enabling clients to produce branded products under their own specifications.
What analytical methods are used for quality control?
Quality control employs HPLC, ICP-MS, and dissolution testing to ensure accuracy, purity, and consistency of active ingredients.
Can Fernish Total be exported to international markets?
Yes, our compliance with FDA, EMA, and PIC/S guidelines enables seamless export to global markets.
What is the minimum order quantity for bulk supply?
Bulk supply options are flexible, with minimum order quantities tailored to client requirements.
How is the supply chain managed for global distribution?
Our supply chain includes real-time tracking, redundant inventory systems, and partnerships with freight forwarders to ensure reliable delivery.
Are there options for private label manufacturing?
Yes, we offer private label manufacturing services, allowing clients to brand products under their own specifications.
What support is available for regulatory documentation?
Our team provides full regulatory documentation, including batch certificates, stability data, and compliance reports for global markets.
