01 1JUNGBUNZLAUER LADENBURG GMBH Ladenburg DE
01 1Potassium citrate
01 1Switzerland
01 1Valid
Certificate Number : CEP 2011-388 - Rev 03
Status : Valid
Issue Date : 2024-05-15
Type : Chemical
Substance Number : 400
19
PharmaCompass offers a list of Potassium Citrate 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 Citrate manufacturer or Potassium Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Potassium Citrate manufacturer or Potassium Citrate supplier.
PharmaCompass also assists you with knowing the Potassium Citrate API Price utilized in the formulation of products. Potassium Citrate API Price is not always fixed or binding as the Potassium Citrate Price is obtained through a variety of data sources. The Potassium Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Litocit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Litocit, including repackagers and relabelers. The FDA regulates Litocit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Litocit API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Litocit supplier is an individual or a company that provides Litocit active pharmaceutical ingredient (API) or Litocit finished formulations upon request. The Litocit suppliers may include Litocit API manufacturers, exporters, distributors and traders.
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A Litocit CEP of the European Pharmacopoeia monograph is often referred to as a Litocit Certificate of Suitability (COS). The purpose of a Litocit CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Litocit EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Litocit to their clients by showing that a Litocit CEP has been issued for it. The manufacturer submits a Litocit CEP (COS) as part of the market authorization procedure, and it takes on the role of a Litocit CEP holder for the record. Additionally, the data presented in the Litocit CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Litocit DMF.
A Litocit CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Litocit CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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