01 1Derivados Quimicos sau
01 1Flutamide
01 1Spain
Registration Number : 217MF11174
Registrant's Address : Camino de Pliego, No. 150, Alcantarilla, 30820, Murcia, Spain
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2019-10-11
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PharmaCompass offers a list of Flutamide 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 Flutamide manufacturer or Flutamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flutamide manufacturer or Flutamide supplier.
PharmaCompass also assists you with knowing the Flutamide API Price utilized in the formulation of products. Flutamide API Price is not always fixed or binding as the Flutamide Price is obtained through a variety of data sources. The Flutamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prostacur manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prostacur, including repackagers and relabelers. The FDA regulates Prostacur manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prostacur 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 Prostacur manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prostacur supplier is an individual or a company that provides Prostacur active pharmaceutical ingredient (API) or Prostacur finished formulations upon request. The Prostacur suppliers may include Prostacur API manufacturers, exporters, distributors and traders.
click here to find a list of Prostacur 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 Prostacur Drug Master File in Japan (Prostacur JDMF) empowers Prostacur 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 Prostacur JDMF during the approval evaluation for pharmaceutical products. At the time of Prostacur 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 Prostacur suppliers with JDMF on PharmaCompass.
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