Product Description
Discover the must-have Paracetamol IP BP USP DC 90% active pharmaceutical ingredient-your classic solution for pharmaceutical formulations. With peerless compressibility for direct compression, this API boasts savings in production and ensures consistent, astounding performance every batch. Its high purity (90%), excellent bulk density (0.35 - 0.45 g/cm3), and strict microbial control foster top-tier safety and efficacy. Complying with all major pharmacopeial standards, this white crystalline powder is slightly soluble in water, offering flexibility in formulation. Find unparalleled reliability-perfect for analgesic and antipyretic products!
Advantage and Competitive Edge of Paracetamol IP BP USP DC 90%
Paracetamol IP BP USP DC 90% offers a superior advantage with its adaptability for direct compression, minimal impurities, and stringent adherence to global pharmaceutical standards. Its primary competitive advantage lies in its consistent particle size-crucial for efficient tablet manufacturing. Direction of use includes utilizing this API in the formulation of analgesic and antipyretic medications. This ensures improved process efficiency, time savings, and a dependable therapeutic effect.
Quotation, Supply, and Certification Details for Paracetamol IP BP USP DC 90%
FOB Port options are versatile to ensure seamless supply across India or for export needs. Samples are available upon request to validate quality prior to purchase, supporting prudent outlay decisions. Comprehensive certification backs every batch, including ICH compliance and pharmacopeial conformity. Request a quotation according to your requirement and benefit from assured delivery and professional handling for bulk orders.
FAQ's of Paracetamol IP BP USP DC 90% active pharmaceutical ingredient:
Q: How is Paracetamol IP BP USP DC 90% used in pharmaceutical formulations?
A: Paracetamol IP BP USP DC 90% is primarily employed as an active pharmaceutical ingredient (API) in making analgesic and antipyretic medications. Its excellent compressibility makes it suitable for direct compression tablet manufacturing.
Q: What are the benefits of choosing Paracetamol IP BP USP DC 90% as an API?
A: This API provides peerless purity, stringent microbial controls, and compliance with global standards, leading to safer and more effective end products. Its direct compression suitability ensures efficient and cost-effective production.
Q: When should Paracetamol IP BP USP DC 90% be stored and handled with caution?
A: It should always be stored in a dry, cool place away from light to maintain its stability, potency, and ensure a shelf life of up to 5 years.
Q: Where can I obtain certification and analysis documents for this API?
A: Certification and documentation, including compliance with ICH and pharmacopeial standards, are provided with each batch to guarantee quality and traceability.
Q: What is the process for requesting a sample or quotation for bulk supply?
A: To request a sample or obtain a quotation, contact the supplier with your requirements, and you will receive details regarding pricing, supply timelines, and shipping options tailored to your needs.
Q: How does its solubility affect its usage in formulations?
A: Paracetamol IP BP USP DC 90% is slightly soluble in water and easily soluble in alcohol, allowing flexibility in formulation approaches for diverse pharmaceutical products.