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01 Lusochimica S. p. A. (1)
01 Fenoterol hydrobromide (1)
01 Italy (1)
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PharmaCompass offers a list of Fenoterol Hydrobromide 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 Fenoterol Hydrobromide manufacturer or Fenoterol Hydrobromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fenoterol Hydrobromide manufacturer or Fenoterol Hydrobromide supplier.
PharmaCompass also assists you with knowing the Fenoterol Hydrobromide API Price utilized in the formulation of products. Fenoterol Hydrobromide API Price is not always fixed or binding as the Fenoterol Hydrobromide Price is obtained through a variety of data sources. The Fenoterol Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fenoterol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenoterol, including repackagers and relabelers. The FDA regulates Fenoterol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenoterol 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 Fenoterol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fenoterol supplier is an individual or a company that provides Fenoterol active pharmaceutical ingredient (API) or Fenoterol finished formulations upon request. The Fenoterol suppliers may include Fenoterol API manufacturers, exporters, distributors and traders.
click here to find a list of Fenoterol 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 Fenoterol Drug Master File in Japan (Fenoterol JDMF) empowers Fenoterol 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 Fenoterol JDMF during the approval evaluation for pharmaceutical products. At the time of Fenoterol 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 Fenoterol suppliers with JDMF on PharmaCompass.
We have 1 companies offering Fenoterol
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