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API SUPPLIERS
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USDMF
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]The Dow Chemical Company
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PharmaCompass offers a list of Sodium Dicloxacillin 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 Sodium Dicloxacillin manufacturer or Sodium Dicloxacillin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Dicloxacillin manufacturer or Sodium Dicloxacillin supplier.
PharmaCompass also assists you with knowing the Sodium Dicloxacillin API Price utilized in the formulation of products. Sodium Dicloxacillin API Price is not always fixed or binding as the Sodium Dicloxacillin Price is obtained through a variety of data sources. The Sodium Dicloxacillin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ciclex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ciclex, including repackagers and relabelers. The FDA regulates Ciclex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ciclex 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 Ciclex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ciclex supplier is an individual or a company that provides Ciclex active pharmaceutical ingredient (API) or Ciclex finished formulations upon request. The Ciclex suppliers may include Ciclex API manufacturers, exporters, distributors and traders.
click here to find a list of Ciclex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ciclex DMF (Drug Master File) is a document detailing the whole manufacturing process of Ciclex active pharmaceutical ingredient (API) in detail. Different forms of Ciclex DMFs exist exist since differing nations have different regulations, such as Ciclex USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ciclex DMF submitted to regulatory agencies in the US is known as a USDMF. Ciclex USDMF includes data on Ciclex's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ciclex USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ciclex suppliers with USDMF on PharmaCompass.
A Ciclex CEP of the European Pharmacopoeia monograph is often referred to as a Ciclex Certificate of Suitability (COS). The purpose of a Ciclex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ciclex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ciclex to their clients by showing that a Ciclex CEP has been issued for it. The manufacturer submits a Ciclex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ciclex CEP holder for the record. Additionally, the data presented in the Ciclex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ciclex DMF.
A Ciclex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ciclex 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 Ciclex suppliers with CEP (COS) on PharmaCompass.
A Ciclex written confirmation (Ciclex WC) is an official document issued by a regulatory agency to a Ciclex manufacturer, verifying that the manufacturing facility of a Ciclex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ciclex APIs or Ciclex finished pharmaceutical products to another nation, regulatory agencies frequently require a Ciclex WC (written confirmation) as part of the regulatory process.
click here to find a list of Ciclex 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 Ciclex as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ciclex 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 Ciclex 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 Ciclex and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ciclex NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ciclex suppliers with NDC on PharmaCompass.
Ciclex 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 Ciclex 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 Ciclex GMP manufacturer or Ciclex GMP API supplier for your needs.
A Ciclex CoA (Certificate of Analysis) is a formal document that attests to Ciclex's compliance with Ciclex specifications and serves as a tool for batch-level quality control.
Ciclex CoA mostly includes findings from lab analyses of a specific batch. For each Ciclex 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.
Ciclex may be tested according to a variety of international standards, such as European Pharmacopoeia (Ciclex EP), Ciclex JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ciclex USP).
