EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI HUNGARY Ltd. Budapest HU
02 1PHARMACIA & UPJOHN COMPANY LLC Kalamazoo US
01 2Dinoprost trometamol
01 1France
02 1U.S.A
01 2Valid
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R0-CEP 2021-310 - Rev 00
Status : Valid
Issue Date : 2023-02-06
Type : Chemical
Substance Number : 1312
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Certificate Number : CEP 2016-337 - Rev 01
Status : Valid
Issue Date : 2024-01-09
Type : Chemical
Substance Number : 1312
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PharmaCompass offers a list of Dinoprost Tromethamine 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 Dinoprost Tromethamine manufacturer or Dinoprost Tromethamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dinoprost Tromethamine manufacturer or Dinoprost Tromethamine supplier.
PharmaCompass also assists you with knowing the Dinoprost Tromethamine API Price utilized in the formulation of products. Dinoprost Tromethamine API Price is not always fixed or binding as the Dinoprost Tromethamine Price is obtained through a variety of data sources. The Dinoprost Tromethamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prostamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prostamate, including repackagers and relabelers. The FDA regulates Prostamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prostamate 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 Prostamate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prostamate supplier is an individual or a company that provides Prostamate active pharmaceutical ingredient (API) or Prostamate finished formulations upon request. The Prostamate suppliers may include Prostamate API manufacturers, exporters, distributors and traders.
click here to find a list of Prostamate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Prostamate CEP of the European Pharmacopoeia monograph is often referred to as a Prostamate Certificate of Suitability (COS). The purpose of a Prostamate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prostamate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prostamate to their clients by showing that a Prostamate CEP has been issued for it. The manufacturer submits a Prostamate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prostamate CEP holder for the record. Additionally, the data presented in the Prostamate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prostamate DMF.
A Prostamate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prostamate 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 Prostamate suppliers with CEP (COS) on PharmaCompass.
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