API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
USA (Orange Book)
0
Europe
Canada
0
Australia
0
South Africa
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
0
75
PharmaCompass offers a list of Fluvastatin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Fluvastatin manufacturer or Fluvastatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluvastatin manufacturer or Fluvastatin supplier.
PharmaCompass also assists you with knowing the Fluvastatin API Price utilized in the formulation of products. Fluvastatin API Price is not always fixed or binding as the Fluvastatin Price is obtained through a variety of data sources. The Fluvastatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fluvastatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluvastatin, including repackagers and relabelers. The FDA regulates Fluvastatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluvastatin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Fluvastatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluvastatin supplier is an individual or a company that provides Fluvastatin active pharmaceutical ingredient (API) or Fluvastatin finished formulations upon request. The Fluvastatin suppliers may include Fluvastatin API manufacturers, exporters, distributors and traders.
click here to find a list of Fluvastatin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fluvastatin DMF (Drug Master File) is a document detailing the whole manufacturing process of Fluvastatin active pharmaceutical ingredient (API) in detail. Different forms of Fluvastatin DMFs exist exist since differing nations have different regulations, such as Fluvastatin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fluvastatin DMF submitted to regulatory agencies in the US is known as a USDMF. Fluvastatin USDMF includes data on Fluvastatin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fluvastatin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fluvastatin suppliers with USDMF on PharmaCompass.
Fluvastatin Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Fluvastatin GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Fluvastatin GMP manufacturer or Fluvastatin GMP API supplier for your needs.
A Fluvastatin CoA (Certificate of Analysis) is a formal document that attests to Fluvastatin's compliance with Fluvastatin specifications and serves as a tool for batch-level quality control.
Fluvastatin CoA mostly includes findings from lab analyses of a specific batch. For each Fluvastatin CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Fluvastatin may be tested according to a variety of international standards, such as European Pharmacopoeia (Fluvastatin EP), Fluvastatin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fluvastatin USP).