01 1EMNAR PHARMA PRIVATE LIMITED Hyderabad IN
02 1NOVABAY Pte. Ltd Singapore SG
03 1SOLVAY OPERATIONS FRANCE Paris FR
04 1SOLVAY PEROXYTHAI LIMITED Rayong TH
05 1Solvay Quimica, S.L. Martorell ES
01 5Sodium hydrogen carbonate
01 1Belgium
02 2France
03 1India
04 1Italy
01 5Valid
Certificate Number : CEP 2022-467 - Rev 01
Status : Valid
Issue Date : 2023-10-27
Type : Chemical
Substance Number : 195
Certificate Number : CEP 2022-300 - Rev 00
Status : Valid
Issue Date : 2024-02-22
Type : Chemical
Substance Number : 195
Certificate Number : R1-CEP 2006-043 - Rev 00
Status : Valid
Issue Date : 2012-03-13
Type : Chemical
Substance Number : 195
Certificate Number : R0-CEP 2020-228 - Rev 00
Status : Valid
Issue Date : 2022-04-08
Type : Chemical
Substance Number : 195
Certificate Number : R1-CEP 2004-252 - Rev 01
Status : Valid
Issue Date : 2017-01-24
Type : Chemical
Substance Number : 195
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PharmaCompass offers a list of Sodium Bicarbonate 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 Bicarbonate manufacturer or Sodium Bicarbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Bicarbonate manufacturer or Sodium Bicarbonate supplier.
PharmaCompass also assists you with knowing the Sodium Bicarbonate API Price utilized in the formulation of products. Sodium Bicarbonate API Price is not always fixed or binding as the Sodium Bicarbonate Price is obtained through a variety of data sources. The Sodium Bicarbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E-500 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E-500, including repackagers and relabelers. The FDA regulates E-500 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E-500 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 E-500 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E-500 supplier is an individual or a company that provides E-500 active pharmaceutical ingredient (API) or E-500 finished formulations upon request. The E-500 suppliers may include E-500 API manufacturers, exporters, distributors and traders.
click here to find a list of E-500 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A E-500 CEP of the European Pharmacopoeia monograph is often referred to as a E-500 Certificate of Suitability (COS). The purpose of a E-500 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of E-500 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of E-500 to their clients by showing that a E-500 CEP has been issued for it. The manufacturer submits a E-500 CEP (COS) as part of the market authorization procedure, and it takes on the role of a E-500 CEP holder for the record. Additionally, the data presented in the E-500 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the E-500 DMF.
A E-500 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. E-500 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 E-500 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering E-500
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