01 1Piramal Pharma Limited
02 1Viwit Pharmaceutical Co. , Ltd.
03 1Wisdom Pharmaceutical Co. , Ltd.
01 1Fosaprepitant Dimeglumine
02 2Fosaprepitant meglumine
01 2China
02 1U.S.A
Registration Number : 302MF10083
Registrant's Address : Digwal Village (Sy.Nos. 7-70, 70/1 and 70/2), Kohir Mandal, Sangareddy District-502 3...
Initial Date of Registration : 2020-07-16
Latest Date of Registration : 2024-07-31
Registration Number : 305MF10071
Registrant's Address : 369 Shengong Road, Zaozhuang High-tech Park, Shandong, China
Initial Date of Registration : 2023-06-07
Latest Date of Registration : 2023-06-07
Registration Number : 304MF10040
Registrant's Address : No. 18 Qinghua Road, Sanchang, Haimen, Jiangsu, China
Initial Date of Registration : 2022-02-24
Latest Date of Registration : 2022-02-24
A Fosaprepitant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fosaprepitant, including repackagers and relabelers. The FDA regulates Fosaprepitant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fosaprepitant 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 Fosaprepitant manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fosaprepitant supplier is an individual or a company that provides Fosaprepitant active pharmaceutical ingredient (API) or Fosaprepitant finished formulations upon request. The Fosaprepitant suppliers may include Fosaprepitant API manufacturers, exporters, distributors and traders.
click here to find a list of Fosaprepitant 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 Fosaprepitant Drug Master File in Japan (Fosaprepitant JDMF) empowers Fosaprepitant 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 Fosaprepitant JDMF during the approval evaluation for pharmaceutical products. At the time of Fosaprepitant 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 Fosaprepitant suppliers with JDMF on PharmaCompass.
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