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PharmaCompass offers a list of Maltodextrin 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 Maltodextrin manufacturer or Maltodextrin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Maltodextrin manufacturer or Maltodextrin supplier.
PharmaCompass also assists you with knowing the Maltodextrin API Price utilized in the formulation of products. Maltodextrin API Price is not always fixed or binding as the Maltodextrin Price is obtained through a variety of data sources. The Maltodextrin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dextrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextrin, including repackagers and relabelers. The FDA regulates Dextrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextrin 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 Dextrin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dextrin supplier is an individual or a company that provides Dextrin active pharmaceutical ingredient (API) or Dextrin finished formulations upon request. The Dextrin suppliers may include Dextrin API manufacturers, exporters, distributors and traders.
click here to find a list of Dextrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dextrin DMF (Drug Master File) is a document detailing the whole manufacturing process of Dextrin active pharmaceutical ingredient (API) in detail. Different forms of Dextrin DMFs exist exist since differing nations have different regulations, such as Dextrin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dextrin DMF submitted to regulatory agencies in the US is known as a USDMF. Dextrin USDMF includes data on Dextrin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dextrin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dextrin 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 Dextrin Drug Master File in Japan (Dextrin JDMF) empowers Dextrin 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 Dextrin JDMF during the approval evaluation for pharmaceutical products. At the time of Dextrin 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 Dextrin suppliers with JDMF on PharmaCompass.
Dextrin 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 Dextrin 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 Dextrin GMP manufacturer or Dextrin GMP API supplier for your needs.
A Dextrin CoA (Certificate of Analysis) is a formal document that attests to Dextrin's compliance with Dextrin specifications and serves as a tool for batch-level quality control.
Dextrin CoA mostly includes findings from lab analyses of a specific batch. For each Dextrin 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.
Dextrin may be tested according to a variety of international standards, such as European Pharmacopoeia (Dextrin EP), Dextrin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dextrin USP).
