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01 2Sicor Societa (') Italiana Corticosteroidi S. r. l.
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01 1Beclomethasone propionate "Teva / low"
02 1Beclomethasone propionate (Teva)
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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.
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 VANCERIL DOUBLE STRENGTH manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VANCERIL DOUBLE STRENGTH, including repackagers and relabelers. The FDA regulates VANCERIL DOUBLE STRENGTH manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VANCERIL DOUBLE STRENGTH 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 VANCERIL DOUBLE STRENGTH manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A VANCERIL DOUBLE STRENGTH supplier is an individual or a company that provides VANCERIL DOUBLE STRENGTH active pharmaceutical ingredient (API) or VANCERIL DOUBLE STRENGTH finished formulations upon request. The VANCERIL DOUBLE STRENGTH suppliers may include VANCERIL DOUBLE STRENGTH API manufacturers, exporters, distributors and traders.
click here to find a list of VANCERIL DOUBLE STRENGTH 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 VANCERIL DOUBLE STRENGTH Drug Master File in Japan (VANCERIL DOUBLE STRENGTH JDMF) empowers VANCERIL DOUBLE STRENGTH 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 VANCERIL DOUBLE STRENGTH JDMF during the approval evaluation for pharmaceutical products. At the time of VANCERIL DOUBLE STRENGTH 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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