Etorwis TH is a dual-ingredient formulation combining Etrocoxib (60mg) and Thiocolchicoside (4mg) in a single tablet, engineered for stability, uniformity, and optimal bioavailability. The formulation employs advanced excipient systems to ensure compatibility between the two active ingredients, which have distinct pharmacological mechanisms. Etrocoxib, a selective COX-2 inhibitor, is combined with Thiocolchicoside, a muscle relaxant and anti-inflammatory agent, to create a synergistic therapeutic profile. The tablet is manufactured using high-speed compression techniques, ensuring consistent weight, hardness, and disintegration properties. The formulation incorporates excipients such as microcrystalline cellulose, magnesium stearate, and colloidal silicon dioxide to enhance flow, compressibility, and tablet integrity. The final product meets stringent physicochemical requirements, including dissolution testing, disintegration time, and stability under accelerated conditions, ensuring long-term shelf life and consistent performance.
Manufacturing Capability
Our manufacturing infrastructure is designed to meet the demands of high-volume pharmaceutical production, with state-of-the-art facilities compliant with current Good Manufacturing Practices (cGMP). The facility includes a dedicated tablet compression line equipped with high-speed tablet presses, ensuring precise dosing and uniform tablet formation. Sterile processing capabilities are available for critical components, supported by a cleanroom environment with controlled particulate and microbial limits. The production process adheres to ISO 9001 quality management standards, with continuous monitoring of critical parameters such as tablet weight variation, content uniformity, and dissolution profiling. Scalability is achieved through modular production lines, enabling seamless transitions from small-scale trials to bulk manufacturing. Quality systems include real-time data acquisition, automated process controls, and rigorous validation protocols to ensure reproducibility and compliance with regulatory expectations.
Available Strengths and Packaging
Composition: Etrocoxib 60mg + Thiocolchicoside 4mg Tab
Packaging: 10x10 Alu Alu
Etorwis TH is available in a single strength formulation, with each tablet containing 60mg of Etrocoxib and 4mg of Thiocolchicoside. The packaging consists of a 10x10 Alu Alu blister pack, designed for efficient storage, transport, and retail display. The aluminum blister provides a moisture- and light-resistant barrier, ensuring product stability during distribution. This packaging format is ideal for both bulk supply and retail channels, offering convenience for end-users and streamlined logistics for distributors.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive third-party manufacturing services, including private label production and contract manufacturing for pharmaceutical buyers. Our facility is equipped to handle complex formulations and packaging requirements, allowing clients to leverage our expertise while maintaining brand control. Private label manufacturing enables clients to produce under their own brand name, with full customization of packaging, labeling, and dosage forms. Contract manufacturing capabilities include support for API sourcing, formulation development, and regulatory documentation, ensuring compliance with global standards. We also provide flexibility in production scales, accommodating both small batches for market testing and large-volume orders for bulk supply.
Quality Assurance
Our quality assurance framework is 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) for active ingredient quantification, dissolution testing to confirm bioavailability, and microbial limit checks for contamination. In-process controls monitor critical parameters such as tablet hardness, disintegration time, and content uniformity, ensuring consistency across batches. Quality control systems are integrated with advanced data analytics to identify trends and mitigate risks. Compliance with USP, EP, and BP monographs ensures product reliability, while regular internal audits and third-party inspections validate adherence to cGMP and ISO standards.
Regulatory Compliance
We maintain strict compliance with global regulatory frameworks, including current Good Manufacturing Practices (cGMP), World Health Organization (WHO) guidelines, and ISO 9001 and ISO 14001 standards. Our facility is certified for GMP compliance by regulatory authorities in multiple jurisdictions, ensuring adherence to international quality benchmarks. WHO guidelines are incorporated into our manufacturing processes to meet export requirements for markets in Africa, Asia, and Latin America. Additionally, we align with ISO 14001 environmental management standards to minimize ecological impact through sustainable practices. Regulatory documentation, including batch records, stability data, and compliance reports, is maintained to support audits and market access.
Global Supply Capability
Our global supply capability is supported by an extensive international distribution network, enabling reliable delivery to markets across Europe, Asia, Africa, and the Americas. We offer bulk supply capacity to meet the demands of pharmaceutical distributors and exporters, with logistics partners ensuring timely and cost-effective shipping. Supply chain reliability is ensured through redundant inventory management, real-time tracking systems, and partnerships with certified freight forwarders. Our facility is equipped to handle large-scale exports, with compliance-ready documentation to facilitate customs clearance and regulatory approvals. Whether you require small-scale trials or large-volume orders, we provide scalable solutions to support your global business objectives.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners choose us for our combination of expertise, compliance, and scalability. Our facility’s adherence to cGMP, ISO, and WHO standards ensures product quality and regulatory readiness, while our flexible manufacturing capabilities allow customization to meet diverse market needs. We prioritize supply chain reliability, with a proven track record of meeting bulk supply demands and supporting global distribution. Our commitment to innovation, coupled with transparent communication and customer-centric support, positions us as a strategic partner for businesses seeking to expand their pharmaceutical portfolio.
Bulk Supply Inquiry
We offer robust bulk supply capabilities to meet the needs of pharmaceutical manufacturers and distributors. For inquiries regarding bulk orders, please contact our sales team at info@delwishealthcare.com.
FAQs
What manufacturing standards does Etorwis TH adhere to?
Etorwis TH is manufactured in compliance with cGMP, WHO guidelines, and ISO 9001 standards, ensuring quality and consistency across production batches.
Can you produce Etorwis TH in custom packaging formats?
Yes, we offer flexible packaging solutions, including the 10x10 Alu Alu blister pack, and can accommodate custom designs for private label manufacturing.
What is the minimum order quantity for bulk supply?
Minimum order quantities are tailored to client requirements, with options for small-scale trials and large-volume production to support global distribution.
How do you ensure the stability of Etorwis TH during storage?
The 10x10 Alu Alu packaging provides a moisture- and light-resistant barrier, while our stability testing protocols ensure product integrity under accelerated conditions.
What regulatory documentation is provided with bulk orders?
Each shipment includes batch certificates of analysis, stability data, and compliance reports to meet regulatory requirements for export and market access.
Can Etorwis TH be produced under a private label?
Yes, our private label manufacturing services allow clients to produce Etorwis TH under their brand name, with full customization of packaging and labeling.
What is your export capability for Etorwis TH?
We have a global distribution network and compliance-ready documentation to support exports to markets in Europe, Asia, Africa, and the Americas.
How do you handle quality control during the manufacturing process?
In-process controls, including HPLC analysis and dissolution testing, ensure consistent quality, while final batch testing confirms compliance with pharmacopeial standards.
Can you scale production to meet large-volume orders?
Our modular production lines enable seamless scalability, supporting both small-scale trials and bulk manufacturing for global supply.
What support is available for regulatory submissions?
Our team provides regulatory documentation, including batch records and stability data, to assist clients with submissions to local and international authorities.
