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01 1Pharmacia & Upjohn Company Kalamazoo US
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01 1Fluoxymesterone
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01 1U.S.A
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01 1Withdrawn by Holder
Certificate Number : R0-CEP 2000-364 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2001-10-26
Type : TSE
Substance Number :
74
PharmaCompass offers a list of Fluoxymesterone 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 Fluoxymesterone manufacturer or Fluoxymesterone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluoxymesterone manufacturer or Fluoxymesterone supplier.
PharmaCompass also assists you with knowing the Fluoxymesterone API Price utilized in the formulation of products. Fluoxymesterone API Price is not always fixed or binding as the Fluoxymesterone Price is obtained through a variety of data sources. The Fluoxymesterone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Stenox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stenox, including repackagers and relabelers. The FDA regulates Stenox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stenox 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 Stenox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Stenox supplier is an individual or a company that provides Stenox active pharmaceutical ingredient (API) or Stenox finished formulations upon request. The Stenox suppliers may include Stenox API manufacturers, exporters, distributors and traders.
click here to find a list of Stenox suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Stenox CEP of the European Pharmacopoeia monograph is often referred to as a Stenox Certificate of Suitability (COS). The purpose of a Stenox CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Stenox EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Stenox to their clients by showing that a Stenox CEP has been issued for it. The manufacturer submits a Stenox CEP (COS) as part of the market authorization procedure, and it takes on the role of a Stenox CEP holder for the record. Additionally, the data presented in the Stenox CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Stenox DMF.
A Stenox CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Stenox 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 Stenox suppliers with CEP (COS) on PharmaCompass.