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