01 1Pharmacia & Upjohn Company Kalamazoo US
01 1Hydrocortisone-17-Butyrate
01 1U.S.A
01 1Withdrawn by Holder
Certificate Number : R0-CEP 2000-291 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2001-10-24
Type : TSE
Substance Number :
68
PharmaCompass offers a list of Hydrocortisone Butyrate 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 Hydrocortisone Butyrate manufacturer or Hydrocortisone Butyrate supplier for your needs.
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PharmaCompass also assists you with knowing the Hydrocortisone Butyrate API Price utilized in the formulation of products. Hydrocortisone Butyrate API Price is not always fixed or binding as the Hydrocortisone Butyrate Price is obtained through a variety of data sources. The Hydrocortisone Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hydrocortisone 17-Butyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone 17-Butyrate, including repackagers and relabelers. The FDA regulates Hydrocortisone 17-Butyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone 17-Butyrate 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 Hydrocortisone 17-Butyrate supplier is an individual or a company that provides Hydrocortisone 17-Butyrate active pharmaceutical ingredient (API) or Hydrocortisone 17-Butyrate finished formulations upon request. The Hydrocortisone 17-Butyrate suppliers may include Hydrocortisone 17-Butyrate API manufacturers, exporters, distributors and traders.
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A Hydrocortisone 17-Butyrate CEP of the European Pharmacopoeia monograph is often referred to as a Hydrocortisone 17-Butyrate Certificate of Suitability (COS). The purpose of a Hydrocortisone 17-Butyrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hydrocortisone 17-Butyrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hydrocortisone 17-Butyrate to their clients by showing that a Hydrocortisone 17-Butyrate CEP has been issued for it. The manufacturer submits a Hydrocortisone 17-Butyrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hydrocortisone 17-Butyrate CEP holder for the record. Additionally, the data presented in the Hydrocortisone 17-Butyrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hydrocortisone 17-Butyrate DMF.
A Hydrocortisone 17-Butyrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hydrocortisone 17-Butyrate 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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