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PharmaCompass offers a list of Dimetindene 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 Dimetindene manufacturer or Dimetindene supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimetindene manufacturer or Dimetindene supplier.
PharmaCompass also assists you with knowing the Dimetindene API Price utilized in the formulation of products. Dimetindene API Price is not always fixed or binding as the Dimetindene Price is obtained through a variety of data sources. The Dimetindene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dimethindene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dimethindene, including repackagers and relabelers. The FDA regulates Dimethindene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dimethindene 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 Dimethindene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dimethindene supplier is an individual or a company that provides Dimethindene active pharmaceutical ingredient (API) or Dimethindene finished formulations upon request. The Dimethindene suppliers may include Dimethindene API manufacturers, exporters, distributors and traders.
click here to find a list of Dimethindene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dimethindene CEP of the European Pharmacopoeia monograph is often referred to as a Dimethindene Certificate of Suitability (COS). The purpose of a Dimethindene CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dimethindene EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dimethindene to their clients by showing that a Dimethindene CEP has been issued for it. The manufacturer submits a Dimethindene CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dimethindene CEP holder for the record. Additionally, the data presented in the Dimethindene CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dimethindene DMF.
A Dimethindene CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dimethindene CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Dimethindene suppliers with CEP (COS) on PharmaCompass.
A Dimethindene written confirmation (Dimethindene WC) is an official document issued by a regulatory agency to a Dimethindene manufacturer, verifying that the manufacturing facility of a Dimethindene active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dimethindene APIs or Dimethindene finished pharmaceutical products to another nation, regulatory agencies frequently require a Dimethindene WC (written confirmation) as part of the regulatory process.
click here to find a list of Dimethindene suppliers with Written Confirmation (WC) on PharmaCompass.
Dimethindene 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 Dimethindene 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 Dimethindene GMP manufacturer or Dimethindene GMP API supplier for your needs.
A Dimethindene CoA (Certificate of Analysis) is a formal document that attests to Dimethindene's compliance with Dimethindene specifications and serves as a tool for batch-level quality control.
Dimethindene CoA mostly includes findings from lab analyses of a specific batch. For each Dimethindene 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.
Dimethindene may be tested according to a variety of international standards, such as European Pharmacopoeia (Dimethindene EP), Dimethindene JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dimethindene USP).