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