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01 1CURIA SPAIN S.A.U. Boecillo ES
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01 1Etonogestrel
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01 1U.S.A
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01 1Valid
Certificate Number : CEP 2025-093 - Rev 00
Status : Valid
Issue Date : 2025-09-19
Type : Chemical
Substance Number : 3049
92
PharmaCompass offers a list of Etonogestrel 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 Etonogestrel manufacturer or Etonogestrel supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etonogestrel manufacturer or Etonogestrel supplier.
PharmaCompass also assists you with knowing the Etonogestrel API Price utilized in the formulation of products. Etonogestrel API Price is not always fixed or binding as the Etonogestrel Price is obtained through a variety of data sources. The Etonogestrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nexplanon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nexplanon, including repackagers and relabelers. The FDA regulates Nexplanon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nexplanon 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 Nexplanon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nexplanon supplier is an individual or a company that provides Nexplanon active pharmaceutical ingredient (API) or Nexplanon finished formulations upon request. The Nexplanon suppliers may include Nexplanon API manufacturers, exporters, distributors and traders.
click here to find a list of Nexplanon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nexplanon CEP of the European Pharmacopoeia monograph is often referred to as a Nexplanon Certificate of Suitability (COS). The purpose of a Nexplanon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nexplanon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nexplanon to their clients by showing that a Nexplanon CEP has been issued for it. The manufacturer submits a Nexplanon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nexplanon CEP holder for the record. Additionally, the data presented in the Nexplanon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nexplanon DMF.
A Nexplanon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nexplanon 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 Nexplanon suppliers with CEP (COS) on PharmaCompass.