Lezend 10 is a pharmaceutical formulation containing Levocetrizine 10mg as the active ingredient, designed for efficacy and stability in pharmaceutical applications. The formulation is optimized for uniformity, disintegration, and dissolution characteristics, ensuring consistent performance during storage and use. The excipients used in the formulation are selected for their compatibility with Levocetrizine, ensuring minimal interaction that could affect potency or shelf life. The manufacturing process employs advanced tablet compression techniques to achieve precise dosing and tablet integrity. The product is formulated to meet stringent pharmaceutical specifications, including pH compatibility, moisture resistance, and thermal stability, making it suitable for long-term storage and global distribution. The formulation is validated through rigorous analytical testing to ensure compliance with pharmacopeial standards, including USP, EP, and BP.
Manufacturing Capability
Our manufacturing infrastructure is designed to meet the demands of pharmaceutical manufacturers requiring high-quality, scalable production. The facility is equipped with state-of-the-art tablet compression, coating, and packaging lines, capable of producing Levocetrizine 10mg tablets in 10x10 Alu Alu packaging with precision. The production process adheres to current Good Manufacturing Practices (cGMP) and includes sterile processing capabilities for critical stages, ensuring contamination-free output. The facility is certified under ISO 9001 and ISO 14001, reflecting our commitment to quality and environmental responsibility. Production scalability is achieved through modular design and flexible manufacturing systems, allowing for rapid adjustments to meet varying order volumes. Quality systems are integrated throughout the manufacturing process, including real-time monitoring, automated data collection, and traceability mechanisms to ensure product integrity.
Available Strengths and Packaging
Composition: Levocetrizine 10mg
Packaging: 10x10 Alu Alu
Lezend 10 is available in a single strength of 10mg, formulated to meet the requirements of pharmaceutical manufacturers seeking a standardized antihistamine product. The 10x10 Alu Alu packaging ensures optimal protection against moisture, light, and physical damage, making it ideal for storage and transportation. The aluminum blister packaging is designed for durability, compliance with pharmaceutical packaging standards, and ease of use in retail and healthcare settings.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to the needs of pharmaceutical buyers. Our capabilities include private label manufacturing, where we produce branded formulations under a client’s proprietary name, as well as contract manufacturing for generic and branded products. We support global clients by providing end-to-end solutions, from raw material sourcing to finished product packaging. Our team works closely with clients to ensure compliance with regulatory requirements and to meet specific formulation and packaging specifications. Whether you require small-scale prototyping or large-volume production, our flexible manufacturing infrastructure ensures timely delivery without compromising quality.
Quality Assurance
Our quality assurance systems are designed to ensure the highest standards of pharmaceutical excellence. Every batch of Levocetrizine 10mg undergoes rigorous testing, including in-process controls, final product analysis, and stability testing to confirm compliance with pharmacopeial standards. Analytical validation is performed using advanced techniques such as High-Performance Liquid Chromatography (HPLC) and UV spectrophotometry to verify potency, purity, and dissolution rates. Quality control measures are integrated into all stages of production, from raw material inspection to finished product release. Our facility maintains detailed batch records and employs a robust traceability system to ensure transparency and accountability. Compliance with International Council for Harmonisation (ICH) guidelines, United States Pharmacopeia (USP), and European Pharmacopeia (EP) standards ensures that our products meet global regulatory expectations.
Regulatory Compliance
We adhere to stringent regulatory frameworks to ensure our products meet international standards. Our manufacturing processes comply with current Good Manufacturing Practices (cGMP) as mandated by the FDA, EMA, and WHO. The facility is registered with regulatory authorities in key markets, including the United States, EU, and Asia-Pacific regions, ensuring seamless compliance with local and international regulations. Our quality management system is aligned with ISO 9001 and ISO 14001 standards, reflecting our commitment to quality and sustainability. Additionally, we maintain compliance with World Health Organization (WHO) guidelines for pharmaceutical manufacturing, ensuring that our products are suitable for global distribution. Regular audits and inspections by third-party regulatory bodies further validate our adherence to global standards.
Global Supply Capability
Our global supply chain is designed to support pharmaceutical manufacturers, exporters, and distributors with reliable, timely delivery of bulk supplies. We have established international distribution networks that facilitate seamless export to over 50 countries, with logistics partners ensuring compliance with import regulations and customs requirements. Our bulk supply capacity is scalable, allowing us to meet the demands of both small and large-scale clients. The 10x10 Alu Alu packaging is optimized for efficient storage and transportation, reducing logistical complexities and ensuring product integrity during transit. Our supply chain reliability is supported by advanced inventory management systems, real-time tracking, and contingency planning to mitigate disruptions. Whether you require small batch shipments or large-volume bulk orders, our infrastructure ensures consistent supply without compromising quality.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners choose us for our expertise in high-quality formulation, regulatory compliance, and scalable production. Our commitment to cGMP standards, ISO certifications, and WHO guidelines ensures that our products meet the demands of global markets. With a focus on innovation and reliability, we provide tailored solutions that align with the specific needs of our clients. Our ability to deliver bulk supplies efficiently, combined with responsive customer support and transparent communication, makes us a trusted partner in the pharmaceutical industry. By leveraging our manufacturing capabilities and global supply network, clients can achieve cost-effective, compliant, and reliable product distribution.
Bulk Supply Inquiry
We offer reliable bulk supply capabilities for Levocetrizine 10mg tablets in 10x10 Alu Alu packaging. For inquiries regarding bulk orders, pricing, or customization, please contact us at info@delwishealthcare.com.
FAQs
What certifications does your facility hold?
Our facility is certified under ISO 9001, ISO 14001, and complies with cGMP, FDA, EMA, and WHO standards.
Can you customize packaging for Levocetrizine 10mg?
Yes, we offer customization options for packaging, including 10x10 Alu Alu and other formats, based on client specifications.
What regulatory standards does your product meet?
Our product complies with USP, EP, BP, and WHO guidelines, ensuring global market readiness.
How long is the shelf life of Levocetrizine 10mg?
The product has a shelf life of 24 months when stored under recommended conditions.
Can you provide bulk supply for export?
Yes, we offer bulk supply capabilities with export-ready packaging and compliance for international markets.
What is the minimum order quantity for Levocetrizine 10mg?
We accommodate small and large orders, with minimum quantities tailored to client requirements.
Do you offer private label manufacturing?
Yes, we provide private label manufacturing services to produce branded formulations under your brand.
How do you ensure quality during production?
We implement real-time monitoring, batch testing, and traceability systems to ensure consistent quality.
Can you support regulatory approvals for international markets?
Yes, our compliance with global standards facilitates regulatory approvals in target markets.
What is your lead time for production?
Lead times vary based on order volume, but we prioritize timely delivery with clear project timelines.
