01 2Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Beclomethasone propionate "Teva / low"
02 1Beclomethasone propionate (Teva)
01 2Italy
Beclomethasone propionate "Teva/Law"
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Beclomethasone Dipropionate manufacturer or Beclomethasone Dipropionate supplier.
PharmaCompass also assists you with knowing the Beclomethasone Dipropionate API Price utilized in the formulation of products. Beclomethasone Dipropionate API Price is not always fixed or binding as the Beclomethasone Dipropionate Price is obtained through a variety of data sources. The Beclomethasone Dipropionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Viarex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Viarex, including repackagers and relabelers. The FDA regulates Viarex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Viarex 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 Viarex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Viarex supplier is an individual or a company that provides Viarex active pharmaceutical ingredient (API) or Viarex finished formulations upon request. The Viarex suppliers may include Viarex API manufacturers, exporters, distributors and traders.
click here to find a list of Viarex 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 Viarex Drug Master File in Japan (Viarex JDMF) empowers Viarex 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 Viarex JDMF during the approval evaluation for pharmaceutical products. At the time of Viarex 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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