Liverest B Plus is a meticulously formulated suspension combining nine active ingredients, including Tricholine Citrate (500mg), L-Ornithine L-Aspartate (150mg), Silymarin (35mg), and a B-complex blend (Vit B1 1.7mg, Vit B2 1.7mg, Vit B6 1.5mg, Vit B12 1mcg), along with D-Panthenol (5mg) and Niacinamide (3mg). The formulation is designed for stability, solubility, and compatibility in a sugar-free suspension base, ensuring uniform dispersion of active ingredients. The product’s composition is optimized for pharmaceutical relevance, with each component selected for its role in metabolic support, liver function, and nutrient delivery. The suspension’s low viscosity and high dispersibility facilitate consistent dosing and ease of administration. From a manufacturing perspective, the formulation balances excipient compatibility, pH stability, and preservative efficacy to meet stringent pharmaceutical standards. The inclusion of D-Panthenol and Niacinamide enhances the product’s role in cellular repair and antioxidant activity, while the B-complex vitamins support enzymatic pathways critical to metabolic processes.
Manufacturing Capability
Liverest B Plus is manufactured using advanced pharmaceutical infrastructure compliant with current Good Manufacturing Practices (cGMP). The production process employs sterile processing techniques to ensure contamination-free handling, particularly for the suspension formulation. State-of-the-art mixing and homogenization systems guarantee uniform dispersion of active ingredients, while controlled temperature and pH conditions maintain stability during formulation. The facility is equipped with ISO 8洁净度 standards, ensuring particulate control and environmental monitoring. Production scalability is achieved through modular manufacturing lines capable of handling bulk orders while maintaining quality consistency. Automated quality control systems, including in-process testing and final product validation, ensure adherence to specifications. The facility’s quality management system (QMS) is ISO 9001-certified, with documented procedures for change control, deviation management, and corrective actions.
Available Strengths and Packaging
Liverest B Plus is available in a single strength, formulated with the specified composition: Tricholine Citrate 500mg, L-Ornithine L-Aspartate 150mg, Silymarin 35mg, D-Panthenol 5mg, Niacinamide 3mg, Vit B1 1.7mg, Vit B2 1.7mg, Vit B6 1.5mg, Vit B12 1mcg, and a sugar-free suspension base. The product is packaged in 200ml bottles with an outer packaging layer, ensuring safe storage and transport while maintaining product integrity.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing and private label services tailored to pharmaceutical buyers. Our facility supports third-party manufacturing for global clients, enabling customization of dosage forms, packaging, and labeling to meet regional regulatory requirements. We provide end-to-end solutions, from formulation development to final packaging, ensuring compliance with international standards. Our capabilities include small-batch prototyping and large-scale production, accommodating diverse demand levels. For exporters and distributors, we facilitate private label manufacturing, allowing brands to leverage our expertise in quality assurance and regulatory compliance.
Quality Assurance
Liverest B Plus undergoes rigorous quality control systems to ensure consistency and safety. Each batch is subjected to analytical validation, including HPLC, UV spectrophotometry, and dissolution testing, to confirm active ingredient potency and uniformity. In-process testing monitors critical parameters such as pH, viscosity, and microbial load, while final product testing verifies compliance with pharmacopeial standards. Our quality assurance team employs validated methods for impurity detection, stability testing, and sterility assurance (where applicable). All documentation adheres to cGMP requirements, with traceability systems ensuring full transparency across the supply chain.
Regulatory Compliance
Liverest B Plus is manufactured in full compliance with GMP, WHO guidelines, and ISO 9001 standards. The product meets international regulatory frameworks, including FDA, EMA, and ICH guidelines, ensuring global market access. Our facility is certified under ISO 14001 for environmental management and ISO 22000 for food safety, reflecting our commitment to sustainable and safe practices. Regulatory documentation, including DMF submissions and batch records, is prepared to support export compliance. We maintain continuous audits and regulatory updates to align with evolving global standards.
Global Supply Capability
Our export capabilities span over 50 countries, supported by a robust international distribution network and logistics partnerships. Liverest B Plus is supplied in bulk quantities to meet large-scale demand, with flexible packaging options for regional requirements. The 200ml packaging ensures efficient storage and transportation, while our supply chain reliability is bolstered by real-time tracking systems and inventory management. We prioritize compliance with import regulations, including customs documentation and labeling standards, to streamline global distribution. Bulk supply capacity is scalable, with dedicated teams managing order fulfillment, customs clearance, and cross-border logistics.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our expertise in high-quality, compliant production. Our facility’s GMP-certified infrastructure ensures product consistency, while our regulatory compliance services simplify market entry. As a trusted supplier, we offer competitive pricing, rapid turnaround times, and tailored solutions to meet specific business needs. Our commitment to innovation, sustainability, and customer-centric service positions us as a reliable partner for global pharmaceutical markets.
Bulk Supply Inquiry
For bulk supply inquiries, contact our team at info@delwishealthcare.com to discuss customization, pricing, and logistics.
FAQs
What manufacturing standards does Liverest B Plus comply with?
Liverest B Plus is manufactured under cGMP, ISO 9001, and WHO guidelines, ensuring adherence to global pharmaceutical standards.
Can Liverest B Plus be customized for private label manufacturing?
Yes, we offer private label manufacturing services, allowing brands to customize packaging, labeling, and dosage forms.
What is the shelf life of Liverest B Plus?
The product has a shelf life of 24 months when stored under recommended conditions, with stability testing confirmed through accelerated aging studies.
Is Liverest B Plus suitable for export to international markets?
Yes, our compliance with FDA, EMA, and ICH guidelines ensures seamless export to global markets.
What quality control measures are in place for batch testing?
Each batch undergoes HPLC, dissolution testing, and microbial analysis to ensure potency, purity, and safety.
Can Liverest B Plus be produced in larger quantities for bulk supply?
Yes, our scalable manufacturing infrastructure supports bulk production to meet large-scale demand.
What packaging options are available for Liverest B Plus?
The product is available in 200ml bottles with outer packaging, with customization options for regional requirements.
How does your facility ensure sterile processing for suspensions?
Our sterile processing lines include HEPA filtration, laminar airflow systems, and environmental monitoring to prevent contamination.
What regulatory documentation is provided for export compliance?
We supply DMF submissions, batch records, and compliance certificates to support regulatory submissions for international markets.
How can I request a bulk supply of Liverest B Plus?
Contact **info@delwishealthcare.com** to discuss bulk supply options, pricing, and logistics.
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