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API SUPPLIERS
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USDMF
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Global Sales Information
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Doxepin 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 Doxepin manufacturer or Doxepin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Doxepin manufacturer or Doxepin supplier.
PharmaCompass also assists you with knowing the Doxepin API Price utilized in the formulation of products. Doxepin API Price is not always fixed or binding as the Doxepin Price is obtained through a variety of data sources. The Doxepin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zonalon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zonalon, including repackagers and relabelers. The FDA regulates Zonalon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zonalon 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 Zonalon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zonalon supplier is an individual or a company that provides Zonalon active pharmaceutical ingredient (API) or Zonalon finished formulations upon request. The Zonalon suppliers may include Zonalon API manufacturers, exporters, distributors and traders.
click here to find a list of Zonalon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zonalon DMF (Drug Master File) is a document detailing the whole manufacturing process of Zonalon active pharmaceutical ingredient (API) in detail. Different forms of Zonalon DMFs exist exist since differing nations have different regulations, such as Zonalon USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zonalon DMF submitted to regulatory agencies in the US is known as a USDMF. Zonalon USDMF includes data on Zonalon's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zonalon USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zonalon suppliers with USDMF on PharmaCompass.
A Zonalon written confirmation (Zonalon WC) is an official document issued by a regulatory agency to a Zonalon manufacturer, verifying that the manufacturing facility of a Zonalon active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zonalon APIs or Zonalon finished pharmaceutical products to another nation, regulatory agencies frequently require a Zonalon WC (written confirmation) as part of the regulatory process.
click here to find a list of Zonalon suppliers with Written Confirmation (WC) on PharmaCompass.
Zonalon 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 Zonalon 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 Zonalon GMP manufacturer or Zonalon GMP API supplier for your needs.
A Zonalon CoA (Certificate of Analysis) is a formal document that attests to Zonalon's compliance with Zonalon specifications and serves as a tool for batch-level quality control.
Zonalon CoA mostly includes findings from lab analyses of a specific batch. For each Zonalon 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.
Zonalon may be tested according to a variety of international standards, such as European Pharmacopoeia (Zonalon EP), Zonalon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zonalon USP).
