01 2Chemtura Corporation Middlebury US
02 1Mallinckrodt Inc St Louis US
03 1SO.G.I.S Industria Chimica SpA Sospiro IT
01 2Calcium stearate
02 1Calcium stearate, (Code numbers 2246, 2247, 2241)
03 1Sodium stearate
01 1Italy
02 3U.S.A
01 4Valid
Certificate Number : R1-CEP 2001-006 - Rev 00
Status : Valid
Issue Date : 2006-05-31
Type : TSE
Substance Number : 882
Certificate Number : R1-CEP 2001-010 - Rev 00
Status : Valid
Issue Date : 2007-01-25
Type : TSE
Substance Number : 2058
Calcium Stearate, (Code Numbers 2246, 2247, 2241...
Certificate Number : R1-CEP 2000-177 - Rev 01
Status : Valid
Issue Date : 2006-11-15
Type : TSE
Substance Number : 882
Certificate Number : R1-CEP 2001-040 - Rev 01
Status : Valid
Issue Date : 2022-03-03
Type : Chemical and TSE
Substance Number : 882
95
PharmaCompass offers a list of Calcium Stearate API 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 Calcium Stearate API manufacturer or Calcium Stearate API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Stearate API manufacturer or Calcium Stearate API supplier.
PharmaCompass also assists you with knowing the Calcium Stearate API API Price utilized in the formulation of products. Calcium Stearate API API Price is not always fixed or binding as the Calcium Stearate API Price is obtained through a variety of data sources. The Calcium Stearate API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A sodium stearate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of sodium stearate, including repackagers and relabelers. The FDA regulates sodium stearate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. sodium stearate 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 sodium stearate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A sodium stearate supplier is an individual or a company that provides sodium stearate active pharmaceutical ingredient (API) or sodium stearate finished formulations upon request. The sodium stearate suppliers may include sodium stearate API manufacturers, exporters, distributors and traders.
click here to find a list of sodium stearate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A sodium stearate CEP of the European Pharmacopoeia monograph is often referred to as a sodium stearate Certificate of Suitability (COS). The purpose of a sodium stearate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of sodium stearate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of sodium stearate to their clients by showing that a sodium stearate CEP has been issued for it. The manufacturer submits a sodium stearate CEP (COS) as part of the market authorization procedure, and it takes on the role of a sodium stearate CEP holder for the record. Additionally, the data presented in the sodium stearate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the sodium stearate DMF.
A sodium stearate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. sodium stearate 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 sodium stearate suppliers with CEP (COS) on PharmaCompass.
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