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