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 ACALKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ACALKA, including repackagers and relabelers. The FDA regulates ACALKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ACALKA 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 ACALKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ACALKA supplier is an individual or a company that provides ACALKA active pharmaceutical ingredient (API) or ACALKA finished formulations upon request. The ACALKA suppliers may include ACALKA API manufacturers, exporters, distributors and traders.
click here to find a list of ACALKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ACALKA CEP of the European Pharmacopoeia monograph is often referred to as a ACALKA Certificate of Suitability (COS). The purpose of a ACALKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ACALKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ACALKA to their clients by showing that a ACALKA CEP has been issued for it. The manufacturer submits a ACALKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a ACALKA CEP holder for the record. Additionally, the data presented in the ACALKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ACALKA DMF.
A ACALKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ACALKA 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 ACALKA suppliers with CEP (COS) on PharmaCompass.
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