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01 1Pharmacia & Upjohn Company Kalamazoo US
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01 1Estradiol Cypionate
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01 1U.S.A
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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Status : Withdrawn by Holder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 :
83
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 Estrapo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estrapo, including repackagers and relabelers. The FDA regulates Estrapo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estrapo 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 Estrapo manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Estrapo supplier is an individual or a company that provides Estrapo active pharmaceutical ingredient (API) or Estrapo finished formulations upon request. The Estrapo suppliers may include Estrapo API manufacturers, exporters, distributors and traders.
click here to find a list of Estrapo suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Estrapo CEP of the European Pharmacopoeia monograph is often referred to as a Estrapo Certificate of Suitability (COS). The purpose of a Estrapo CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Estrapo EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Estrapo to their clients by showing that a Estrapo CEP has been issued for it. The manufacturer submits a Estrapo CEP (COS) as part of the market authorization procedure, and it takes on the role of a Estrapo CEP holder for the record. Additionally, the data presented in the Estrapo CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Estrapo DMF.
A Estrapo CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Estrapo 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 Estrapo suppliers with CEP (COS) on PharmaCompass.