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PharmaCompass offers a list of Opipramol 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 Opipramol manufacturer or Opipramol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Opipramol manufacturer or Opipramol supplier.
PharmaCompass also assists you with knowing the Opipramol API Price utilized in the formulation of products. Opipramol API Price is not always fixed or binding as the Opipramol Price is obtained through a variety of data sources. The Opipramol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Opipramol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Opipramol, including repackagers and relabelers. The FDA regulates Opipramol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Opipramol 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 Opipramol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Opipramol supplier is an individual or a company that provides Opipramol active pharmaceutical ingredient (API) or Opipramol finished formulations upon request. The Opipramol suppliers may include Opipramol API manufacturers, exporters, distributors and traders.
click here to find a list of Opipramol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Opipramol written confirmation (Opipramol WC) is an official document issued by a regulatory agency to a Opipramol manufacturer, verifying that the manufacturing facility of a Opipramol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Opipramol APIs or Opipramol finished pharmaceutical products to another nation, regulatory agencies frequently require a Opipramol WC (written confirmation) as part of the regulatory process.
click here to find a list of Opipramol suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Opipramol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Opipramol API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Opipramol as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Opipramol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Opipramol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Opipramol suppliers with NDC on PharmaCompass.
Opipramol 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 Opipramol 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 Opipramol GMP manufacturer or Opipramol GMP API supplier for your needs.
A Opipramol CoA (Certificate of Analysis) is a formal document that attests to Opipramol's compliance with Opipramol specifications and serves as a tool for batch-level quality control.
Opipramol CoA mostly includes findings from lab analyses of a specific batch. For each Opipramol 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.
Opipramol may be tested according to a variety of international standards, such as European Pharmacopoeia (Opipramol EP), Opipramol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Opipramol USP).