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ATORVASTATIN

ATORVASTATIN
ATORVASTATIN

ATORVASTATIN Specification

  • Packaging Details
  • HDPE drums with double liners or as required
  • Purity
  • 98%
  • Hazard Code
  • Xn (Harmful)
  • Molecular Formula
  • C33H35FN2O5
  • Usage
  • Lowers cholesterol and triglyceride levels
  • Standard
  • USP/EP/BP
  • Molecular Weight
  • 558.64 g/mol
  • Form
  • Powder
  • Appearance
  • White to off-white crystalline powder
  • Grade
  • Pharmaceutical Grade
  • Solubility
  • Slightly soluble in water, soluble in methanol and ethanol
  • Product Name
  • ATORVASTATIN
  • Melting Point
  • 159-160C
  • Therapeutic Category
  • Antihyperlipidemic
  • Storage
  • Store in a cool, dry place
  • CAS No
  • 134523-00-5
  • Shelf Life
  • 24 months
  • Certificate of Analysis
  • Available upon request
 
 

About ATORVASTATIN



Take advantage of ravishing ATORVASTATIN, a meritorious and polished antihyperlipidemic agent in high demand. Offered as a white to off-white crystalline powder, its purity reaches 98%. Suitable for pharmaceutical applications, it meets USP/EP/BP standards. With reduced solubility in water yet readily soluble in methanol and ethanol, it provides reliable results. Its extended shelf life of 24 months, secured in HDPE drums with double liners, enhances safety. Store in a cool, dry place and request a Certificate of Analysis for complete assurance. Exporter, manufacturer, supplier, and trader based in India.

Applications and Commercial Uses of ATORVASTATIN

ATORVASTATIN is extensively used by pharmaceutical manufacturers, research laboratories, and clinical specialists. As an antihyperlipidemic agent, its application spans the formulation of tablets and capsules designed to lower cholesterol and triglyceride levels. Commercial uses include bulk production, contract research, and clinical trials. This product benefits both academic institutions and commercial enterprises seeking reliable ingredients for cardiovascular medications, ensuring therapeutic efficacy and consistency.


Export, Domestic Market and Secure Shipment of ATORVASTATIN

ATORVASTATINs main export markets encompass North America, Europe, and Southeast Asia, reflecting its global demand. In India, the domestic market includes pharmaceutical firms and medical suppliers, supporting nationwide healthcare initiatives. Secure shipping procedures and robust packaging with HDPE drums ensure safe and compliant delivery of every shipment. Flexible payment terms help facilitate smooth business transactions, further promoting its reach among international buyers and domestic clients.


FAQs of ATORVASTATIN:


Q: How should ATORVASTATIN powder be stored for maximum shelf life?

A: ATORVASTATIN powder should be stored in a cool, dry place within its HDPE drums with double liners to maintain its quality and maximize its 24-month shelf life.

Q: What is the main usage and benefit of ATORVASTATIN in the pharmaceutical industry?

A: ATORVASTATIN is primarily used to lower cholesterol and triglyceride levels, serving as a potent antihyperlipidemic agent in the manufacture of cardiovascular medications.

Q: When can I request a Certificate of Analysis for ATORVASTATIN shipments?

A: A Certificate of Analysis is available upon request with any shipment or bulk order of ATORVASTATIN, ensuring product quality and compliance with standards.

Q: Where is ATORVASTATIN manufactured and supplied from?

A: ATORVASTATIN is manufactured, exported, and supplied by industry-leading companies based in India, with secure international and domestic shipments.

Q: What process is used for packaging ATORVASTATIN powder for shipment?

A: ATORVASTATIN powder is packed in HDPE drums with double liners, or as per customer requirements, ensuring safe, secure transport and product integrity.

Q: How is the products quality ensured before export or domestic distribution?

A: Quality is verified through adherence to USP/EP/BP standards and can be further assured by requesting a Certificate of Analysis prior to shipment.

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