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API SUPPLIERS
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Evonik
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Faran Shimi Pharmaceutical
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Microlex e.U
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Bold Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pluviaendo
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ABOUT THIS PAGE
46
PharmaCompass offers a list of Dextrans 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 Dextrans manufacturer or Dextrans supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dextrans manufacturer or Dextrans supplier.
PharmaCompass also assists you with knowing the Dextrans API Price utilized in the formulation of products. Dextrans API Price is not always fixed or binding as the Dextrans Price is obtained through a variety of data sources. The Dextrans Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DEXTRAN SULFATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DEXTRAN SULFATE, including repackagers and relabelers. The FDA regulates DEXTRAN SULFATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DEXTRAN SULFATE 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 DEXTRAN SULFATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DEXTRAN SULFATE supplier is an individual or a company that provides DEXTRAN SULFATE active pharmaceutical ingredient (API) or DEXTRAN SULFATE finished formulations upon request. The DEXTRAN SULFATE suppliers may include DEXTRAN SULFATE API manufacturers, exporters, distributors and traders.
click here to find a list of DEXTRAN SULFATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DEXTRAN SULFATE DMF (Drug Master File) is a document detailing the whole manufacturing process of DEXTRAN SULFATE active pharmaceutical ingredient (API) in detail. Different forms of DEXTRAN SULFATE DMFs exist exist since differing nations have different regulations, such as DEXTRAN SULFATE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DEXTRAN SULFATE DMF submitted to regulatory agencies in the US is known as a USDMF. DEXTRAN SULFATE USDMF includes data on DEXTRAN SULFATE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DEXTRAN SULFATE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DEXTRAN SULFATE 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 DEXTRAN SULFATE Drug Master File in Japan (DEXTRAN SULFATE JDMF) empowers DEXTRAN SULFATE 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 DEXTRAN SULFATE JDMF during the approval evaluation for pharmaceutical products. At the time of DEXTRAN SULFATE 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 DEXTRAN SULFATE suppliers with JDMF on PharmaCompass.
A DEXTRAN SULFATE CEP of the European Pharmacopoeia monograph is often referred to as a DEXTRAN SULFATE Certificate of Suitability (COS). The purpose of a DEXTRAN SULFATE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DEXTRAN SULFATE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DEXTRAN SULFATE to their clients by showing that a DEXTRAN SULFATE CEP has been issued for it. The manufacturer submits a DEXTRAN SULFATE CEP (COS) as part of the market authorization procedure, and it takes on the role of a DEXTRAN SULFATE CEP holder for the record. Additionally, the data presented in the DEXTRAN SULFATE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DEXTRAN SULFATE DMF.
A DEXTRAN SULFATE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DEXTRAN SULFATE 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 DEXTRAN SULFATE suppliers with CEP (COS) 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 DEXTRAN SULFATE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for DEXTRAN SULFATE 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 DEXTRAN SULFATE 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 DEXTRAN SULFATE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a DEXTRAN SULFATE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of DEXTRAN SULFATE suppliers with NDC on PharmaCompass.
DEXTRAN SULFATE 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 DEXTRAN SULFATE 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 DEXTRAN SULFATE GMP manufacturer or DEXTRAN SULFATE GMP API supplier for your needs.
A DEXTRAN SULFATE CoA (Certificate of Analysis) is a formal document that attests to DEXTRAN SULFATE's compliance with DEXTRAN SULFATE specifications and serves as a tool for batch-level quality control.
DEXTRAN SULFATE CoA mostly includes findings from lab analyses of a specific batch. For each DEXTRAN SULFATE 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.
DEXTRAN SULFATE may be tested according to a variety of international standards, such as European Pharmacopoeia (DEXTRAN SULFATE EP), DEXTRAN SULFATE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DEXTRAN SULFATE USP).
