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Slide All

Slide All is a combination pharmaceutical tablet containing Paracetamol 500mg, Phenylephrine Hydrochloride 10mg, and C.P. Maleate 2mg, designed for therapeutic efficacy in pharmaceutical applications requiring analgesic, antipyretic, and decongestant properties.

Composition

Paracetamol 500mg + Phenylephrine Hydrochloride 10mg + C.P. Maleate 2mg Tab

Pack Size

20x10 Blister

Slide All is a multi-ingredient pharmaceutical tablet formulated with Paracetamol (500mg) as the primary analgesic and antipyretic agent, Phenylephrine Hydrochloride (10mg) as a sympathomimetic decongestant, and C.P. Maleate (2mg) as a central-acting antihistamine. The formulation is designed to ensure optimal dissolution, stability, and bioavailability of active ingredients. The tablet’s composition is carefully balanced to achieve synergistic therapeutic effects while maintaining compatibility between components. Manufacturing involves advanced excipient selection, compression techniques, and coating processes to ensure uniformity, disintegration time, and robustness against environmental factors. The formulation adheres to strict pharmaceutical standards, ensuring consistent performance and quality across batches.

Manufacturing Capability

Our manufacturing infrastructure is equipped with state-of-the-art facilities compliant with current Good Manufacturing Practices (cGMP) and ISO 9001:2015 standards. The production process includes sterile processing capabilities for sensitive formulations, ensuring contamination-free environments. Advanced tablet compression machines, high-speed coating systems, and automated packaging lines enable precise control over dosage uniformity, tablet hardness, and disintegration parameters. The facility supports scalable production, with the capacity to meet bulk supply demands for global markets. Quality systems include real-time monitoring, calibration protocols, and documentation frameworks to ensure traceability and regulatory compliance.

Available Strengths and Packaging

Slide All is available in a single strength: Paracetamol 500mg + Phenylephrine Hydrochloride 10mg + C.P. Maleate 2mg. The product is packaged in 20x10 blister packs, ensuring secure, tamper-evident storage and distribution. This packaging format is ideal for retail and institutional use, offering convenience and compliance with pharmaceutical storage requirements.

Contract Manufacturing / Third Party Manufacturing

As a trusted manufacturer, we offer comprehensive contract manufacturing, private label production, and third-party manufacturing services tailored to pharmaceutical buyers. Our capabilities include formulation development, API integration, and full-scale production of customized dosage forms. We support clients in meeting specific regulatory and market requirements, ensuring flexibility in product design and packaging. Our services are ideal for brands seeking to expand their portfolio without in-house manufacturing constraints.

Quality Assurance

Our quality assurance framework encompasses rigorous batch testing, analytical validation, and adherence to pharmaceutical quality standards. Each batch undergoes testing for dissolution, content uniformity, and impurity analysis using High-Performance Liquid Chromatography (HPLC) and other advanced techniques. Microbial testing, stability studies, and packaging integrity assessments are conducted to ensure product safety and efficacy. Comprehensive documentation, including batch records and certificates of analysis (CoA), is provided to meet regulatory and client requirements.

Regulatory Compliance

Slide All complies with global regulatory frameworks, including cGMP, WHO guidelines, and ISO 9001:2015 standards. Our manufacturing processes adhere to strict quality control measures to meet the requirements of regulatory authorities such as the FDA, EMA, and PIC/S. The product is formulated and produced in compliance with international pharmacopeial standards, ensuring suitability for export and global distribution.

Global Supply Capability

We have a robust international distribution network and the capacity to supply bulk quantities of Slide All to markets worldwide. Our logistics partnerships ensure timely delivery, compliance with import regulations, and seamless supply chain management. The facility is equipped to handle large-scale orders, with reliable inventory management systems to guarantee consistent supply. We prioritize supply chain resilience, ensuring minimal disruption and adherence to delivery timelines.

Why Choose Us

Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our expertise in high-quality production, regulatory compliance, and scalable supply solutions. Our commitment to cGMP standards, advanced manufacturing technology, and global market access positions us as a reliable partner for bulk supply and customized pharmaceutical needs. We offer competitive pricing, transparent documentation, and dedicated support to meet the evolving demands of the pharmaceutical industry.

Bulk Supply Inquiry

For bulk supply inquiries, contact our team at info@delwishealthcare.com.

FAQs

  1. What manufacturing standards does Slide All comply with?

    Slide All is manufactured in compliance with cGMP, ISO 9001:2015, and WHO guidelines, ensuring adherence to global pharmaceutical quality standards.

  2. Can Slide All be produced in different packaging formats?

    While the standard packaging is 20x10 blister packs, we offer customization options for alternative packaging formats upon request.

  3. What is the shelf life of Slide All?

    Slide All has a shelf life of 24 months when stored under recommended conditions, as validated through stability studies.

  4. Does your facility support sterile manufacturing processes?

    Yes, our facility is equipped with sterile processing capabilities to ensure contamination-free production of sensitive formulations.

  5. Can you provide documentation for regulatory submissions?

    We provide comprehensive documentation, including batch records, certificates of analysis (CoA), and regulatory compliance reports for global market access.

  6. What is your minimum order quantity for bulk supply?

    We accommodate bulk supply requests with flexible order quantities, tailored to meet the needs of pharmaceutical buyers.

  7. How do you ensure the consistency of active ingredients?

    Our formulation process includes rigorous analytical validation, content uniformity testing, and HPLC analysis to ensure consistent active ingredient levels.

  8. Can Slide All be customized for private label manufacturing?

    Yes, we offer private label manufacturing services, allowing clients to brand the product under their own label while maintaining quality standards.

  9. What is your export capability?

    We have a global distribution network and export capabilities to meet the needs of international markets, with compliance to regional import regulations.

  10. How do you handle supply chain disruptions?

    Our supply chain management systems include contingency planning, diversified supplier networks, and real-time monitoring to ensure uninterrupted supply.

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