01 1JUNGBUNZLAUER LADENBURG GMBH Ladenburg DE
01 1Sodium citrate dihydrate
01 1Switzerland
01 1Valid
Certificate Number : CEP 2018-273 - Rev 06
Status : Valid
Issue Date : 2025-07-11
Type : Chemical
Substance Number : 412
49
PharmaCompass offers a list of Sodium 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 Sodium Citrate manufacturer or Sodium Citrate supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Citrate API Price utilized in the formulation of products. Sodium Citrate API Price is not always fixed or binding as the Sodium Citrate Price is obtained through a variety of data sources. The Sodium Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Citrosodine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Citrosodine, including repackagers and relabelers. The FDA regulates Citrosodine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Citrosodine 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 Citrosodine supplier is an individual or a company that provides Citrosodine active pharmaceutical ingredient (API) or Citrosodine finished formulations upon request. The Citrosodine suppliers may include Citrosodine API manufacturers, exporters, distributors and traders.
click here to find a list of Citrosodine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Citrosodine CEP of the European Pharmacopoeia monograph is often referred to as a Citrosodine Certificate of Suitability (COS). The purpose of a Citrosodine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Citrosodine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Citrosodine to their clients by showing that a Citrosodine CEP has been issued for it. The manufacturer submits a Citrosodine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Citrosodine CEP holder for the record. Additionally, the data presented in the Citrosodine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Citrosodine DMF.
A Citrosodine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Citrosodine 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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