EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
02 2Kyowa Pharma Chemical Co., Ltd.
01 2Dinoprostone
02 1Ginoproston
01 1France
02 2Japan
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 230MF10136
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2018-09-21
Latest Date of Registration : 2018-09-21
Registration Number : 307MF10024
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2025-02-07
Latest Date of Registration : 2025-02-07
Registration Number : 230MF10070
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2018-06-07
Latest Date of Registration : 2018-06-07
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PharmaCompass offers a list of Dinoprostone 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 Dinoprostone manufacturer or Dinoprostone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dinoprostone manufacturer or Dinoprostone supplier.
PharmaCompass also assists you with knowing the Dinoprostone API Price utilized in the formulation of products. Dinoprostone API Price is not always fixed or binding as the Dinoprostone Price is obtained through a variety of data sources. The Dinoprostone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PGE2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PGE2, including repackagers and relabelers. The FDA regulates PGE2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PGE2 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 PGE2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PGE2 supplier is an individual or a company that provides PGE2 active pharmaceutical ingredient (API) or PGE2 finished formulations upon request. The PGE2 suppliers may include PGE2 API manufacturers, exporters, distributors and traders.
click here to find a list of PGE2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The PGE2 Drug Master File in Japan (PGE2 JDMF) empowers PGE2 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the PGE2 JDMF during the approval evaluation for pharmaceutical products. At the time of PGE2 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of PGE2 suppliers with JDMF on PharmaCompass.
We have 2 companies offering PGE2
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