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