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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
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01 5Sodium hydrogen carbonate
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01 1Belgium
02 2France
03 1India
04 1Italy
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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 5006-97-3 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 5006-97-3, including repackagers and relabelers. The FDA regulates 5006-97-3 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 5006-97-3 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 5006-97-3 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 5006-97-3 supplier is an individual or a company that provides 5006-97-3 active pharmaceutical ingredient (API) or 5006-97-3 finished formulations upon request. The 5006-97-3 suppliers may include 5006-97-3 API manufacturers, exporters, distributors and traders.
click here to find a list of 5006-97-3 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 5006-97-3 CEP of the European Pharmacopoeia monograph is often referred to as a 5006-97-3 Certificate of Suitability (COS). The purpose of a 5006-97-3 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 5006-97-3 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 5006-97-3 to their clients by showing that a 5006-97-3 CEP has been issued for it. The manufacturer submits a 5006-97-3 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 5006-97-3 CEP holder for the record. Additionally, the data presented in the 5006-97-3 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 5006-97-3 DMF.
A 5006-97-3 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 5006-97-3 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 5006-97-3 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering 5006-97-3
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