01 1Lusochimica S. p. A.
01 1Fenoterol hydrobromide
01 1Italy
Registration Number : 218MF10961
Registrant's Address : Via Giotto 9,23871 Lomagna(LC)Italy
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2008-11-04
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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.
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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 Berotek manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Berotek, including repackagers and relabelers. The FDA regulates Berotek manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Berotek API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Berotek supplier is an individual or a company that provides Berotek active pharmaceutical ingredient (API) or Berotek finished formulations upon request. The Berotek suppliers may include Berotek API manufacturers, exporters, distributors and traders.
click here to find a list of Berotek 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 Berotek Drug Master File in Japan (Berotek JDMF) empowers Berotek 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 Berotek JDMF during the approval evaluation for pharmaceutical products. At the time of Berotek 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 Berotek suppliers with JDMF on PharmaCompass.
