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PharmaCompass offers a list of Eperisone 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 Eperisone manufacturer or Eperisone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Eperisone manufacturer or Eperisone supplier.
PharmaCompass also assists you with knowing the Eperisone API Price utilized in the formulation of products. Eperisone API Price is not always fixed or binding as the Eperisone Price is obtained through a variety of data sources. The Eperisone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eperisone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eperisone, including repackagers and relabelers. The FDA regulates Eperisone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eperisone 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 Eperisone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eperisone supplier is an individual or a company that provides Eperisone active pharmaceutical ingredient (API) or Eperisone finished formulations upon request. The Eperisone suppliers may include Eperisone API manufacturers, exporters, distributors and traders.
click here to find a list of Eperisone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eperisone DMF (Drug Master File) is a document detailing the whole manufacturing process of Eperisone active pharmaceutical ingredient (API) in detail. Different forms of Eperisone DMFs exist exist since differing nations have different regulations, such as Eperisone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eperisone DMF submitted to regulatory agencies in the US is known as a USDMF. Eperisone USDMF includes data on Eperisone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eperisone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Eperisone suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Eperisone Drug Master File in Japan (Eperisone JDMF) empowers Eperisone API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Eperisone JDMF during the approval evaluation for pharmaceutical products. At the time of Eperisone JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Eperisone suppliers with JDMF on PharmaCompass.
Eperisone 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 Eperisone 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 Eperisone GMP manufacturer or Eperisone GMP API supplier for your needs.
A Eperisone CoA (Certificate of Analysis) is a formal document that attests to Eperisone's compliance with Eperisone specifications and serves as a tool for batch-level quality control.
Eperisone CoA mostly includes findings from lab analyses of a specific batch. For each Eperisone 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.
Eperisone may be tested according to a variety of international standards, such as European Pharmacopoeia (Eperisone EP), Eperisone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eperisone USP).
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