EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Reset all filters
01 1EUROAPI Hungary Ltd.
02 2Kyowa Pharma Chemical Co., Ltd.
Reset all filters
01 2Dinoprostone
02 1Ginoproston
Reset all filters
01 1France
02 2Japan
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 : 230MF10070
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2018-06-07
Latest Date of Registration : 2018-06-07
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
61
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 P2E manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of P2E, including repackagers and relabelers. The FDA regulates P2E manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. P2E 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 P2E manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A P2E supplier is an individual or a company that provides P2E active pharmaceutical ingredient (API) or P2E finished formulations upon request. The P2E suppliers may include P2E API manufacturers, exporters, distributors and traders.
click here to find a list of P2E 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 P2E Drug Master File in Japan (P2E JDMF) empowers P2E 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 P2E JDMF during the approval evaluation for pharmaceutical products. At the time of P2E 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 P2E suppliers with JDMF on PharmaCompass.
We have 2 companies offering P2E
Get in contact with the supplier of your choice: