01 1Pharmacia & Upjohn Company Kalamazoo US
01 1Cortisone acetate
01 1U.S.A
01 1Expired
Certificate Number : R0-CEP 2001-128 - Rev 00
Status : Expired
Issue Date : 2002-05-17
Type : TSE
Substance Number : 321
75
PharmaCompass offers a list of Cortisone 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 Cortisone manufacturer or Cortisone supplier for your needs.
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PharmaCompass also assists you with knowing the Cortisone API Price utilized in the formulation of products. Cortisone API Price is not always fixed or binding as the Cortisone Price is obtained through a variety of data sources. The Cortisone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A S2559_Selleck manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of S2559_Selleck, including repackagers and relabelers. The FDA regulates S2559_Selleck manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. S2559_Selleck 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 S2559_Selleck supplier is an individual or a company that provides S2559_Selleck active pharmaceutical ingredient (API) or S2559_Selleck finished formulations upon request. The S2559_Selleck suppliers may include S2559_Selleck API manufacturers, exporters, distributors and traders.
click here to find a list of S2559_Selleck suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A S2559_Selleck CEP of the European Pharmacopoeia monograph is often referred to as a S2559_Selleck Certificate of Suitability (COS). The purpose of a S2559_Selleck CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of S2559_Selleck EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of S2559_Selleck to their clients by showing that a S2559_Selleck CEP has been issued for it. The manufacturer submits a S2559_Selleck CEP (COS) as part of the market authorization procedure, and it takes on the role of a S2559_Selleck CEP holder for the record. Additionally, the data presented in the S2559_Selleck CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the S2559_Selleck DMF.
A S2559_Selleck CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. S2559_Selleck 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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