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PharmaCompass offers a list of Chlorhexidine HCl 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 Chlorhexidine HCl manufacturer or Chlorhexidine HCl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorhexidine HCl manufacturer or Chlorhexidine HCl supplier.
PharmaCompass also assists you with knowing the Chlorhexidine HCl API Price utilized in the formulation of products. Chlorhexidine HCl API Price is not always fixed or binding as the Chlorhexidine HCl Price is obtained through a variety of data sources. The Chlorhexidine HCl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride, including repackagers and relabelers. The FDA regulates 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride 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 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride supplier is an individual or a company that provides 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride active pharmaceutical ingredient (API) or 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride finished formulations upon request. The 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride suppliers may include 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride active pharmaceutical ingredient (API) in detail. Different forms of 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride DMFs exist exist since differing nations have different regulations, such as 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride USDMF includes data on 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride Drug Master File in Japan (1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride JDMF) empowers 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride 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 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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A 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride Certificate of Suitability (COS). The purpose of a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride to their clients by showing that a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CEP has been issued for it. The manufacturer submits a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CEP holder for the record. Additionally, the data presented in the 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride DMF.
A 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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A 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride written confirmation (1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride WC) is an official document issued by a regulatory agency to a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride manufacturer, verifying that the manufacturing facility of a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride APIs or 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride WC (written confirmation) as part of the regulatory process.
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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 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride 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 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride 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 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride NDC to their finished compounded human drug products, they may choose to do so.
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1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride 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 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride 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 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride GMP manufacturer or 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride GMP API supplier for your needs.
A 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CoA (Certificate of Analysis) is a formal document that attests to 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride's compliance with 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride specifications and serves as a tool for batch-level quality control.
1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride 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.
1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride EP), 1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1,6-Di(N-p-chlorophenyl-diguanido) hexane dihydrochloride USP).
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