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01 2EUROAPI Hungary Ltd.
02 1Kanto Chemical Co., Ltd.
03 1YS Life Science Co. , Ltd.
01 2Limaprost Alfadex
02 2Limaprost alfadex
01 2France
02 1Japan
03 1South Korea
Registration Number : 304MF10134
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2022-09-21
Latest Date of Registration : 2022-09-21
Registration Number : 219MF10023
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2007-01-22
Latest Date of Registration : 2012-10-03
Registration Number : 218MF10300
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2016-02-18
Registration Number : 222MF10166
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2010-06-04
Latest Date of Registration : 2010-06-04
A Limaprost Alfadex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Limaprost Alfadex, including repackagers and relabelers. The FDA regulates Limaprost Alfadex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Limaprost Alfadex 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 Limaprost Alfadex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Limaprost Alfadex supplier is an individual or a company that provides Limaprost Alfadex active pharmaceutical ingredient (API) or Limaprost Alfadex finished formulations upon request. The Limaprost Alfadex suppliers may include Limaprost Alfadex API manufacturers, exporters, distributors and traders.
click here to find a list of Limaprost Alfadex 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 Limaprost Alfadex Drug Master File in Japan (Limaprost Alfadex JDMF) empowers Limaprost Alfadex 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 Limaprost Alfadex JDMF during the approval evaluation for pharmaceutical products. At the time of Limaprost Alfadex 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 Limaprost Alfadex suppliers with JDMF on PharmaCompass.
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