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The Journey of Statins: From API Synthesis to Drug Product in Cholesterol Management

The journey of a pharmaceutical drug, from its initial chemical synthesis as an Active Pharmaceutical Ingredient (API) to a patient-ready medication, is a complex and highly regulated process. For statins, a class of drugs pivotal in cholesterol management, this journey is particularly critical given their widespread use in preventing and treating cardiovascular diseases.

Take Simvastatin, for instance, a potent lipid-lowering agent commonly used for hypercholesterolemia treatment. Its development and manufacturing begin with the synthesis of the pure Simvastatin API, identified by its CAS number 79902-63-9. This initial stage demands meticulous precision and stringent quality control to achieve the desired 99% purity, a hallmark of a reliable Simvastatin API manufacturer China.

The API is then formulated into various dosage forms, such as tablets, ensuring optimal bioavailability and stability. This involves careful selection of excipients and rigorous testing to guarantee the integrity and efficacy of the final product. Manufacturers must ensure that every batch of Simvastatin meets global pharmaceutical standards, making the Simvastatin API supplier selection a key decision in the drug development lifecycle.

For companies looking to buy Simvastatin CAS 79902-63-9 in bulk, understanding the full scope of the manufacturing process from their supplier is crucial. It’s not just about the Simvastatin price, but also about the integrity of the supply chain, adherence to Good Manufacturing Practices (GMP), and the ability to scale production while maintaining consistent quality. This ensures continuous access to medication for patients requiring coronary heart disease prevention.

The seamless integration of high-quality API production and advanced drug formulation is what ultimately enables statins like Simvastatin to play their essential role in global public health, helping millions manage their cholesterol and reduce the risk of debilitating heart conditions. The commitment to excellence at every stage of development and manufacturing is non-negotiable.

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NINGBO INNO PHARMCHEM CO.,LTD. was established in 2007. It is committed to the R&D, production and sales of raw materials, pharmaceutical intermediates and fine chemicals. We striving to create a high-efficiency and high-quality integrated chemical service platform to better serve domestic and foreign customers.

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WHY CHOSE US?

1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;

2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;

3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).

FAQ

  • A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.

  • A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.

  • A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.

CONTACT US
Should you need to contact us; you may call during regular business hours, Monday through Friday, 8am – 6 pm.
NINGBO INNO PHARMCHEM CO.,LTD.
Address: No.163 Ruiqing Rd.,Ningbo 315000 China
Phone: 86-574-87319282
Fax: 86-574-27912196
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