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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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 Propaderm Forte manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propaderm Forte, including repackagers and relabelers. The FDA regulates Propaderm Forte manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propaderm Forte 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 Propaderm Forte supplier is an individual or a company that provides Propaderm Forte active pharmaceutical ingredient (API) or Propaderm Forte finished formulations upon request. The Propaderm Forte suppliers may include Propaderm Forte API manufacturers, exporters, distributors and traders.
click here to find a list of Propaderm Forte 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 Propaderm Forte Drug Master File in Japan (Propaderm Forte JDMF) empowers Propaderm Forte 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 Propaderm Forte JDMF during the approval evaluation for pharmaceutical products. At the time of Propaderm Forte 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 Propaderm Forte suppliers with JDMF on PharmaCompass.
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