01 1Pharmacia & Upjohn Company Kalamazoo US
01 1Estradiol Cypionate
01 1U.S.A
01 1Withdrawn by Holder
Certificate Number : R0-CEP 2000-394 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2001-11-05
Type : TSE
Substance Number :
88
PharmaCompass offers a list of Estradiol Cypionate 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 Estradiol Cypionate manufacturer or Estradiol Cypionate supplier for your needs.
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PharmaCompass also assists you with knowing the Estradiol Cypionate API Price utilized in the formulation of products. Estradiol Cypionate API Price is not always fixed or binding as the Estradiol Cypionate Price is obtained through a variety of data sources. The Estradiol Cypionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Estro-Depo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estro-Depo, including repackagers and relabelers. The FDA regulates Estro-Depo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estro-Depo 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 Estro-Depo supplier is an individual or a company that provides Estro-Depo active pharmaceutical ingredient (API) or Estro-Depo finished formulations upon request. The Estro-Depo suppliers may include Estro-Depo API manufacturers, exporters, distributors and traders.
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A Estro-Depo CEP of the European Pharmacopoeia monograph is often referred to as a Estro-Depo Certificate of Suitability (COS). The purpose of a Estro-Depo CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Estro-Depo EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Estro-Depo to their clients by showing that a Estro-Depo CEP has been issued for it. The manufacturer submits a Estro-Depo CEP (COS) as part of the market authorization procedure, and it takes on the role of a Estro-Depo CEP holder for the record. Additionally, the data presented in the Estro-Depo CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Estro-Depo DMF.
A Estro-Depo CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Estro-Depo 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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