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PharmaCompass offers a list of Disodium Hydrogen Phosphate 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 Disodium Hydrogen Phosphate manufacturer or Disodium Hydrogen Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Disodium Hydrogen Phosphate manufacturer or Disodium Hydrogen Phosphate supplier.
PharmaCompass also assists you with knowing the Disodium Hydrogen Phosphate API Price utilized in the formulation of products. Disodium Hydrogen Phosphate API Price is not always fixed or binding as the Disodium Hydrogen Phosphate Price is obtained through a variety of data sources. The Disodium Hydrogen Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 04273_SIAL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 04273_SIAL, including repackagers and relabelers. The FDA regulates 04273_SIAL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 04273_SIAL 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 04273_SIAL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 04273_SIAL supplier is an individual or a company that provides 04273_SIAL active pharmaceutical ingredient (API) or 04273_SIAL finished formulations upon request. The 04273_SIAL suppliers may include 04273_SIAL API manufacturers, exporters, distributors and traders.
click here to find a list of 04273_SIAL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 04273_SIAL DMF (Drug Master File) is a document detailing the whole manufacturing process of 04273_SIAL active pharmaceutical ingredient (API) in detail. Different forms of 04273_SIAL DMFs exist exist since differing nations have different regulations, such as 04273_SIAL USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 04273_SIAL DMF submitted to regulatory agencies in the US is known as a USDMF. 04273_SIAL USDMF includes data on 04273_SIAL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 04273_SIAL USDMF is kept confidential to protect the manufacturer’s intellectual property.
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A 04273_SIAL CEP of the European Pharmacopoeia monograph is often referred to as a 04273_SIAL Certificate of Suitability (COS). The purpose of a 04273_SIAL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 04273_SIAL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 04273_SIAL to their clients by showing that a 04273_SIAL CEP has been issued for it. The manufacturer submits a 04273_SIAL CEP (COS) as part of the market authorization procedure, and it takes on the role of a 04273_SIAL CEP holder for the record. Additionally, the data presented in the 04273_SIAL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 04273_SIAL DMF.
A 04273_SIAL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 04273_SIAL 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 04273_SIAL 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 04273_SIAL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 04273_SIAL 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 04273_SIAL 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 04273_SIAL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 04273_SIAL NDC to their finished compounded human drug products, they may choose to do so.
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04273_SIAL 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 04273_SIAL 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 04273_SIAL GMP manufacturer or 04273_SIAL GMP API supplier for your needs.
A 04273_SIAL CoA (Certificate of Analysis) is a formal document that attests to 04273_SIAL's compliance with 04273_SIAL specifications and serves as a tool for batch-level quality control.
04273_SIAL CoA mostly includes findings from lab analyses of a specific batch. For each 04273_SIAL 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.
04273_SIAL may be tested according to a variety of international standards, such as European Pharmacopoeia (04273_SIAL EP), 04273_SIAL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (04273_SIAL USP).