01 2Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Beclomethasone propionate "Teva / low"
02 1Beclomethasone propionate (Teva)
01 2Italy
Beclomethasone propionate "Teva/Rho"
Registration Number : 218MF10626
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2006-07-20
Latest Date of Registration : 2006-07-20
Beclomethasone dipropionate (Teva)
Registration Number : 218MF10532
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2006-06-01
Latest Date of Registration : 2006-06-01
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PharmaCompass offers a list of Beclomethasone Dipropionate 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 Beclomethasone Dipropionate manufacturer or Beclomethasone Dipropionate supplier for your needs.
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A Asmabec Clickhaler manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Asmabec Clickhaler, including repackagers and relabelers. The FDA regulates Asmabec Clickhaler manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Asmabec Clickhaler 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 Asmabec Clickhaler supplier is an individual or a company that provides Asmabec Clickhaler active pharmaceutical ingredient (API) or Asmabec Clickhaler finished formulations upon request. The Asmabec Clickhaler suppliers may include Asmabec Clickhaler API manufacturers, exporters, distributors and traders.
click here to find a list of Asmabec Clickhaler 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 Asmabec Clickhaler Drug Master File in Japan (Asmabec Clickhaler JDMF) empowers Asmabec Clickhaler 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 Asmabec Clickhaler JDMF during the approval evaluation for pharmaceutical products. At the time of Asmabec Clickhaler JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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