API Suppliers
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
EU WC
Listed Suppliers
USA (Orange Book)
0
Europe
Canada
0
Australia
0
South Africa
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
0
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
88
PharmaCompass offers a list of Mizolastine 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 Mizolastine manufacturer or Mizolastine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mizolastine manufacturer or Mizolastine supplier.
PharmaCompass also assists you with knowing the Mizolastine API Price utilized in the formulation of products. Mizolastine API Price is not always fixed or binding as the Mizolastine Price is obtained through a variety of data sources. The Mizolastine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mizolastine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mizolastine, including repackagers and relabelers. The FDA regulates Mizolastine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mizolastine 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 Mizolastine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mizolastine supplier is an individual or a company that provides Mizolastine active pharmaceutical ingredient (API) or Mizolastine finished formulations upon request. The Mizolastine suppliers may include Mizolastine API manufacturers, exporters, distributors and traders.
click here to find a list of Mizolastine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mizolastine written confirmation (Mizolastine WC) is an official document issued by a regulatory agency to a Mizolastine manufacturer, verifying that the manufacturing facility of a Mizolastine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Mizolastine APIs or Mizolastine finished pharmaceutical products to another nation, regulatory agencies frequently require a Mizolastine WC (written confirmation) as part of the regulatory process.
click here to find a list of Mizolastine suppliers with Written Confirmation (WC) on PharmaCompass.
Mizolastine 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 Mizolastine 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 Mizolastine GMP manufacturer or Mizolastine GMP API supplier for your needs.
A Mizolastine CoA (Certificate of Analysis) is a formal document that attests to Mizolastine's compliance with Mizolastine specifications and serves as a tool for batch-level quality control.
Mizolastine CoA mostly includes findings from lab analyses of a specific batch. For each Mizolastine 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.
Mizolastine may be tested according to a variety of international standards, such as European Pharmacopoeia (Mizolastine EP), Mizolastine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Mizolastine USP).