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ABOUT THIS PAGE
12
PharmaCompass offers a list of Sodium Hydrogenphosphate Dihydrate 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 Hydrogenphosphate Dihydrate manufacturer or Sodium Hydrogenphosphate Dihydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Hydrogenphosphate Dihydrate manufacturer or Sodium Hydrogenphosphate Dihydrate supplier.
PharmaCompass also assists you with knowing the Sodium Hydrogenphosphate Dihydrate API Price utilized in the formulation of products. Sodium Hydrogenphosphate Dihydrate API Price is not always fixed or binding as the Sodium Hydrogenphosphate Dihydrate Price is obtained through a variety of data sources. The Sodium Hydrogenphosphate Dihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Disodium hydrogen phosphate dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disodium hydrogen phosphate dihydrate, including repackagers and relabelers. The FDA regulates Disodium hydrogen phosphate dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disodium hydrogen phosphate dihydrate 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 Disodium hydrogen phosphate dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disodium hydrogen phosphate dihydrate supplier is an individual or a company that provides Disodium hydrogen phosphate dihydrate active pharmaceutical ingredient (API) or Disodium hydrogen phosphate dihydrate finished formulations upon request. The Disodium hydrogen phosphate dihydrate suppliers may include Disodium hydrogen phosphate dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Disodium hydrogen phosphate dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Disodium hydrogen phosphate dihydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Disodium hydrogen phosphate dihydrate active pharmaceutical ingredient (API) in detail. Different forms of Disodium hydrogen phosphate dihydrate DMFs exist exist since differing nations have different regulations, such as Disodium hydrogen phosphate dihydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Disodium hydrogen phosphate dihydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Disodium hydrogen phosphate dihydrate USDMF includes data on Disodium hydrogen phosphate dihydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Disodium hydrogen phosphate dihydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Disodium hydrogen phosphate dihydrate suppliers with USDMF 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 Disodium hydrogen phosphate dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Disodium hydrogen phosphate dihydrate 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 Disodium hydrogen phosphate dihydrate 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 Disodium hydrogen phosphate dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Disodium hydrogen phosphate dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Disodium hydrogen phosphate dihydrate suppliers with NDC on PharmaCompass.
Disodium hydrogen phosphate dihydrate 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 Disodium hydrogen phosphate dihydrate 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 Disodium hydrogen phosphate dihydrate GMP manufacturer or Disodium hydrogen phosphate dihydrate GMP API supplier for your needs.
A Disodium hydrogen phosphate dihydrate CoA (Certificate of Analysis) is a formal document that attests to Disodium hydrogen phosphate dihydrate's compliance with Disodium hydrogen phosphate dihydrate specifications and serves as a tool for batch-level quality control.
Disodium hydrogen phosphate dihydrate CoA mostly includes findings from lab analyses of a specific batch. For each Disodium hydrogen phosphate dihydrate 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.
Disodium hydrogen phosphate dihydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Disodium hydrogen phosphate dihydrate EP), Disodium hydrogen phosphate dihydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Disodium hydrogen phosphate dihydrate USP).
