01 1MSN Laboratories Private Limited.
02 1Tateyama Chemical Co., Ltd.
01 1Ambrisentan
02 1Ambrisentan
01 1India
02 1Japan
Registration Number : 302MF10087
Registrant's Address : Plot No: C-24, Sanath Nagar Industrial Estate, Sanath Nagar, Hyderabad, Telangana, In...
Initial Date of Registration : 2020-07-22
Latest Date of Registration : 2021-05-10
Registration Number : 302MF10090
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2020-07-29
Latest Date of Registration : 2022-01-11
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PharmaCompass offers a list of Ambrisentan 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 Ambrisentan manufacturer or Ambrisentan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ambrisentan manufacturer or Ambrisentan supplier.
PharmaCompass also assists you with knowing the Ambrisentan API Price utilized in the formulation of products. Ambrisentan API Price is not always fixed or binding as the Ambrisentan Price is obtained through a variety of data sources. The Ambrisentan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Volibris manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Volibris, including repackagers and relabelers. The FDA regulates Volibris manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Volibris 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 Volibris manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Volibris supplier is an individual or a company that provides Volibris active pharmaceutical ingredient (API) or Volibris finished formulations upon request. The Volibris suppliers may include Volibris API manufacturers, exporters, distributors and traders.
click here to find a list of Volibris 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 Volibris Drug Master File in Japan (Volibris JDMF) empowers Volibris 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 Volibris JDMF during the approval evaluation for pharmaceutical products. At the time of Volibris 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 Volibris suppliers with JDMF on PharmaCompass.
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