01 1Sucampo Pharma LLC
02 1Yonsung Fine Chemicals Co. , Ltd.
01 1Isopropyl unoprostone
02 1Isopropyl unoprostone "production-only"
01 1South Korea
02 1U.S.A
Registration Number : 227MF10230
Registrant's Address : 2-6-4 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2015-09-03
Latest Date of Registration : 2015-09-03
Isopropyl Unoprostone (For manufacturing purposes only)
Registration Number : 219MF10370
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2007-12-13
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PharmaCompass offers a list of Isopropyl Unoprostone 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 Isopropyl Unoprostone manufacturer or Isopropyl Unoprostone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isopropyl Unoprostone manufacturer or Isopropyl Unoprostone supplier.
PharmaCompass also assists you with knowing the Isopropyl Unoprostone API Price utilized in the formulation of products. Isopropyl Unoprostone API Price is not always fixed or binding as the Isopropyl Unoprostone Price is obtained through a variety of data sources. The Isopropyl Unoprostone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 13,14-Dihydro-15-keto-20-ethyl-PGF2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 13,14-Dihydro-15-keto-20-ethyl-PGF2, including repackagers and relabelers. The FDA regulates 13,14-Dihydro-15-keto-20-ethyl-PGF2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 13,14-Dihydro-15-keto-20-ethyl-PGF2 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 13,14-Dihydro-15-keto-20-ethyl-PGF2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 13,14-Dihydro-15-keto-20-ethyl-PGF2 supplier is an individual or a company that provides 13,14-Dihydro-15-keto-20-ethyl-PGF2 active pharmaceutical ingredient (API) or 13,14-Dihydro-15-keto-20-ethyl-PGF2 finished formulations upon request. The 13,14-Dihydro-15-keto-20-ethyl-PGF2 suppliers may include 13,14-Dihydro-15-keto-20-ethyl-PGF2 API manufacturers, exporters, distributors and traders.
click here to find a list of 13,14-Dihydro-15-keto-20-ethyl-PGF2 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 13,14-Dihydro-15-keto-20-ethyl-PGF2 Drug Master File in Japan (13,14-Dihydro-15-keto-20-ethyl-PGF2 JDMF) empowers 13,14-Dihydro-15-keto-20-ethyl-PGF2 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 13,14-Dihydro-15-keto-20-ethyl-PGF2 JDMF during the approval evaluation for pharmaceutical products. At the time of 13,14-Dihydro-15-keto-20-ethyl-PGF2 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 13,14-Dihydro-15-keto-20-ethyl-PGF2 suppliers with JDMF on PharmaCompass.
We have 2 companies offering 13,14-Dihydro-15-keto-20-ethyl-PGF2
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