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