Vizolam P is a fixed-dose combination tablet containing Alprazolam (0.25mg) and Propranolol HCL (20mg), formulated to ensure optimal stability, bioavailability, and therapeutic efficacy. The active ingredients are combined using advanced solid dosage formulation techniques, including direct compression and coating processes, to achieve uniform drug distribution and enhanced shelf life. Alprazolam, a benzodiazepine, is incorporated as a free base, while Propranolol HCL is formulated as a hydrochloride salt to ensure solubility and consistent release. The excipients used in the formulation, including microcrystalline cellulose, magnesium stearate, and hypromellose, are selected for their compatibility with the active pharmaceutical ingredients (APIs) and their ability to maintain tablet integrity under varied storage conditions. The formulation is designed to meet stringent pharmaceutical requirements, ensuring minimal degradation of APIs during storage and transportation.
Manufacturing Capability
Our manufacturing infrastructure is equipped with state-of-the-art facilities designed to produce high-quality pharmaceutical products in compliance with global standards. The production process for Vizolam P adheres to Good Manufacturing Practice (GMP) guidelines, ensuring sterility, consistency, and safety throughout the manufacturing cycle. The facility includes advanced tablet compression machines, coating systems, and automated packaging lines capable of handling large-scale production. Sterile processing capabilities are maintained through controlled environment manufacturing (CEM) techniques, ensuring contamination-free production of dosage forms. The facility is certified under ISO 9001:2015 and ISO 14001:2015, reflecting our commitment to quality management and environmental sustainability. Production scalability is achieved through modular design and flexible manufacturing systems, allowing seamless transitions from small batch trials to large-scale commercial production. Rigorous quality systems, including real-time monitoring and data integrity protocols, ensure consistent product quality and regulatory compliance.
Available Strengths and Packaging
Composition: Alprazolam 0.25mg + Propranolol HCL 20mg Tab
Packaging: 4x5x10 Blister
Vizolam P is available in a single strength formulation, combining Alprazolam 0.25mg and Propranolol HCL 20mg in a blister pack format. The 4x5x10 blister packaging ensures secure storage, tamper-evident protection, and efficient dispensing, making it ideal for both institutional and retail distribution. The packaging design complies with international pharmaceutical standards, ensuring durability and compliance with regulatory requirements for over-the-counter and prescription drug distribution.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing, private label, and third-party manufacturing services tailored to meet the needs of pharmaceutical buyers. Our capabilities include the production of custom formulations, dosage forms, and packaging solutions, allowing clients to leverage our expertise while maintaining brand control. We support both domestic and international clients by providing end-to-end manufacturing services, from API sourcing and formulation development to packaging and distribution. Our flexible manufacturing infrastructure enables rapid prototyping and scalability, ensuring timely delivery of high-quality products. Clients can benefit from our expertise in regulatory compliance, quality assurance, and cost-effective production, making us a preferred partner for pharmaceutical manufacturers seeking to expand their product portfolios.
Quality Assurance
Our quality assurance systems are designed to ensure the highest standards of pharmaceutical excellence. Every batch of Vizolam P undergoes rigorous testing, including high-performance liquid chromatography (HPLC) for API quantification, dissolution testing to confirm drug release profiles, and microbial limit testing to ensure sterility. Analytical validation protocols are implemented to verify the accuracy, precision, and reproducibility of test results. Quality control measures are integrated throughout the manufacturing process, from raw material sourcing to finished product release, ensuring compliance with pharmacopoeial standards such as USP and EP. Our facility is equipped with advanced analytical instrumentation and validated testing procedures to meet the demands of regulatory audits and client specifications.
Regulatory Compliance
We ensure full compliance with Good Manufacturing Practice (GMP) standards, World Health Organization (WHO) guidelines, and international regulatory frameworks. Our manufacturing processes adhere to ISO 9001:2015 and ISO 14001:2015 certifications, demonstrating our commitment to quality and environmental responsibility. Products are manufactured in compliance with the requirements of the U.S. FDA, EMA, and other global regulatory bodies, ensuring eligibility for export to markets worldwide. Our quality management system includes documentation, traceability, and continuous improvement practices to meet the evolving demands of the pharmaceutical industry. Regulatory compliance is a core component of our operations, enabling seamless product approval and distribution across international markets.
Global Supply Capability
Our global supply capability is supported by an extensive international distribution network and robust logistics infrastructure. We provide bulk supply options to meet the demands of pharmaceutical distributors, exporters, and contract manufacturers, ensuring timely delivery to key markets. Our supply chain is designed for reliability, with strategic partnerships in logistics and customs clearance to facilitate smooth cross-border transactions. Bulk supply capacity is optimized through scalable production and efficient inventory management, allowing us to meet large-volume orders without compromising quality or delivery timelines. Our export capabilities are further enhanced by compliance with international trade regulations, ensuring seamless compliance with import/export documentation and customs requirements.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our expertise in high-quality, compliant manufacturing. Our commitment to GMP standards, regulatory compliance, and scalable production ensures reliable supply chains and product consistency. As a trusted manufacturer, we offer competitive pricing, fast turnaround times, and tailored solutions to meet the unique needs of our clients. Our global supply network and experienced team provide end-to-end support, from formulation development to international distribution. By partnering with us, clients gain access to a reliable, compliant, and scalable manufacturing solution that meets the demands of the global pharmaceutical market.
Bulk Supply Inquiry
For bulk supply inquiries, please contact our sales team at info@delwishealthcare.com.
FAQs
What manufacturing standards does Vizolam P comply with?
Vizolam P is manufactured in compliance with GMP, WHO, and ISO standards, ensuring adherence to global pharmaceutical quality requirements.
Can Vizolam P be customized for specific packaging formats?
Yes, we offer flexible packaging solutions, including blister packs, to meet client-specific requirements.
What is the shelf life of Vizolam P?
The shelf life of Vizolam P is typically 24 months when stored under recommended conditions.
Does your facility support sterile manufacturing processes?
Yes, our facility is equipped with sterile processing capabilities to ensure contamination-free production.
Can you provide bulk supply for international markets?
Yes, we offer bulk supply solutions with global distribution capabilities, supporting export to key markets.
What quality control measures are in place for Vizolam P?
Each batch undergoes rigorous testing, including HPLC, dissolution, and microbial limit tests, to ensure product integrity.
Are there options for private label manufacturing?
Yes, we provide private label manufacturing services to help clients brand and distribute their products.
How do you ensure regulatory compliance for international exports?
Our facility adheres to global regulatory frameworks, and we support compliance with FDA, EMA, and other international standards.
What is the minimum order quantity for bulk supply?
Minimum order quantities are flexible and can be discussed based on client requirements and production capacity.
Can you accommodate urgent production timelines?
Yes, our scalable manufacturing infrastructure allows for expedited production to meet urgent client demands.
