Argidel Sachet is a meticulously formulated pharmaceutical product combining L-Arginine (3gm), Zinc Sulphate Monohydrate (10mg), and Folic Acid (2.5mg) in an orange-flavored sachet. The formulation is designed to ensure stability, solubility, and uniform dispersion of active ingredients during manufacturing. L-Arginine, a semi-essential amino acid, is incorporated to enhance bioavailability and support metabolic processes. Zinc Sulphate Monohydrate serves as a source of zinc, a critical micronutrient for enzymatic functions, while Folic Acid provides essential B-vitamin support for cellular proliferation. The orange flavor is added as a functional excipient to improve palatability without compromising the integrity of the active components. The sachet format ensures convenient dosing and portability, making it suitable for both clinical and over-the-counter applications. The formulation adheres to strict pharmaceutical standards, ensuring compatibility with excipients, pH stability, and compatibility with packaging materials.
Manufacturing Capability
Our manufacturing infrastructure is equipped to produce high-quality pharmaceutical products like Argidel Sachet with precision and efficiency. The facility features advanced aseptic processing capabilities, ensuring sterile handling of ingredients and final product. Production adheres to current Good Manufacturing Practices (cGMP) and includes state-of-the-art equipment for blending, granulation, and sachet filling. The facility is designed for scalability, enabling seamless transitions from small-scale trials to bulk production. Quality systems are integrated throughout the manufacturing process, including real-time monitoring of critical parameters such as temperature, humidity, and particle size. The facility also complies with ISO 9001 standards, ensuring consistent product quality and process reliability.
Available Strengths and Packaging
The composition of Argidel Sachet is standardized to L-Arginine 3gm, Zinc Sulphate Monohydrate 10mg, and Folic Acid 2.5mg, with the orange flavor as a functional excipient. The product is available in a 5gm X10 sachet packaging format, ensuring optimal dosing and storage. This packaging design balances portability with shelf-life stability, making it ideal for distribution in diverse markets.
Contract Manufacturing / Third Party Manufacturing
As a trusted pharmaceutical manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to meet the needs of global buyers. Our facility is equipped to handle private label manufacturing, allowing clients to brand and distribute products under their own names. We specialize in producing high-quality pharmaceutical sachets, ensuring compliance with regulatory standards and customer specifications. Our team of experts provides end-to-end solutions, from formulation development to packaging and labeling, ensuring seamless integration with clients’ supply chains. Whether you require small-batch trials or large-scale production, our scalable infrastructure and flexible manufacturing capabilities ensure timely delivery of premium-quality products.
Quality Assurance
Our quality assurance systems are designed to ensure the highest standards of pharmaceutical excellence. Every batch of Argidel Sachet undergoes rigorous testing, including physical, chemical, and microbiological analyses. Key parameters such as active ingredient content, pH, disintegration time, and microbial load are validated using advanced analytical techniques like High-Performance Liquid Chromatography (HPLC) and spectroscopy. Batch testing is conducted in accordance with International Council for Harmonisation (ICH) guidelines, ensuring consistency and safety. Additionally, our quality control team performs routine audits and maintains detailed documentation to comply with Good Manufacturing Practices (GMP) and pharmacopoeial standards.
Regulatory Compliance
We adhere to stringent regulatory frameworks to ensure global market accessibility. Our manufacturing processes comply with current Good Manufacturing Practices (cGMP), World Health Organization (WHO) guidelines, and ISO 9001 quality management standards. Products are validated against pharmacopoeial monographs, including USP, EP, and BP, ensuring compliance with international regulatory requirements. Our facility is certified for export to key markets, including the EU, US, and Asia-Pacific regions, with documentation aligned to FDA, EMA, and other regulatory bodies. This compliance ensures seamless approval processes and market entry for pharmaceutical buyers.
Global Supply Capability
Our global supply chain is designed to meet the demands of international markets with reliability and efficiency. We offer bulk supply capabilities, supporting large-scale distribution through established logistics networks. Our export infrastructure includes compliance with international shipping regulations, temperature-controlled transportation, and documentation for customs clearance. The 5gm X10 sachet packaging is optimized for global distribution, ensuring product integrity during transit. With a focus on supply chain resilience, we maintain strategic partnerships with freight forwarders and logistics providers to ensure timely delivery to destinations worldwide.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners choose us for our expertise in high-quality pharmaceutical production, regulatory compliance, and scalable manufacturing solutions. Our facility’s adherence to GMP, ISO, and WHO standards ensures product consistency and global market readiness. We offer tailored services, including private label manufacturing and bulk supply options, to meet diverse client needs. Our commitment to innovation, reliability, and customer support positions us as a preferred partner for businesses seeking to expand their product portfolios in competitive markets.
Bulk Supply Inquiry
For bulk supply inquiries, please contact us at info@delwishealthcare.com. Our team is dedicated to providing seamless solutions for pharmaceutical buyers seeking reliable, high-quality products.
FAQs
What certifications does your facility hold for pharmaceutical manufacturing?
Our facility is certified under cGMP, ISO 9001, and WHO guidelines, ensuring compliance with global regulatory standards.
Can you customize the packaging for Argidel Sachet?
Yes, we offer customization options for packaging, including different sachet sizes and labeling, to meet specific client requirements.
What is the shelf life of Argidel Sachet?
The product has a shelf life of 24 months when stored in optimal conditions (temperature 15–25°C, humidity <60%).
Are your products compliant with FDA and EMA regulations?
Yes, all products are manufactured to meet FDA, EMA, and other international regulatory standards for pharmaceutical quality.
What quality control measures are in place for Argidel Sachet?
Each batch undergoes rigorous testing, including HPLC analysis, microbial testing, and stability studies, to ensure product integrity.
Can you provide bulk supply for international markets?
Yes, we offer bulk supply capabilities with a global distribution network to support exports to over 50 countries.
What is the minimum order quantity for Argidel Sachet?
Minimum order quantities are flexible and can be discussed based on production capacity and client requirements.
How do you ensure the stability of the orange flavor in the sachet?
The orange flavor is selected for its chemical stability and compatibility with the active ingredients, ensuring product integrity during storage.
Can you assist with regulatory documentation for export?
Yes, we provide complete regulatory documentation, including certificates of analysis and compliance reports, to facilitate international exports.
What is your lead time for production and delivery?
Lead times vary based on order size and production schedule. We provide detailed timelines upon order confirmation to ensure timely delivery.
