01 2Wisdom Pharmaceutical Co. , Ltd.
01 1Fasudil Hydrochloride Hydrate
02 1Fasudil hydrochloride hydrate
01 2China
Registration Number : 228MF10174
Registrant's Address : No. 18 Qinghua Road, Sanchang, Haimen, Jiangsu, China
Initial Date of Registration : 2016-08-29
Latest Date of Registration : 2016-08-29
Registration Number : 231MF10048
Registrant's Address : No. 18 Qinghua Road, Sanchang, Haimen, Jiangsu, China
Initial Date of Registration : 2019-02-15
Latest Date of Registration : 2022-03-02
A Fasudil Hydrochloride Hydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fasudil Hydrochloride Hydrate, including repackagers and relabelers. The FDA regulates Fasudil Hydrochloride Hydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fasudil Hydrochloride Hydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Fasudil Hydrochloride Hydrate supplier is an individual or a company that provides Fasudil Hydrochloride Hydrate active pharmaceutical ingredient (API) or Fasudil Hydrochloride Hydrate finished formulations upon request. The Fasudil Hydrochloride Hydrate suppliers may include Fasudil Hydrochloride Hydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Fasudil Hydrochloride Hydrate 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 Fasudil Hydrochloride Hydrate Drug Master File in Japan (Fasudil Hydrochloride Hydrate JDMF) empowers Fasudil Hydrochloride Hydrate 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 Fasudil Hydrochloride Hydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Fasudil Hydrochloride Hydrate 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 Fasudil Hydrochloride Hydrate suppliers with JDMF on PharmaCompass.
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