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