01 1Zhejiang Ausun Pharmaceutical Co. , Ltd.
01 1Macitentan
01 1China
Registration Number : 307MF10112
Registrant's Address : No. 5, Donghai 4th Avenue, Zhejiang Chemical Materials Base Linhai Zone, Zhejiang, Ch...
Initial Date of Registration : 2025-09-03
Latest Date of Registration : 2025-09-03
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PharmaCompass offers a list of Macitentan 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 Macitentan manufacturer or Macitentan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Macitentan manufacturer or Macitentan supplier.
PharmaCompass also assists you with knowing the Macitentan API Price utilized in the formulation of products. Macitentan API Price is not always fixed or binding as the Macitentan Price is obtained through a variety of data sources. The Macitentan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A opsumit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of opsumit, including repackagers and relabelers. The FDA regulates opsumit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. opsumit 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 opsumit manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A opsumit supplier is an individual or a company that provides opsumit active pharmaceutical ingredient (API) or opsumit finished formulations upon request. The opsumit suppliers may include opsumit API manufacturers, exporters, distributors and traders.
click here to find a list of opsumit 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 opsumit Drug Master File in Japan (opsumit JDMF) empowers opsumit 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 opsumit JDMF during the approval evaluation for pharmaceutical products. At the time of opsumit 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 opsumit suppliers with JDMF on PharmaCompass.
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