01 2Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Beclomethasone propionate "Teva / low"
02 1Beclomethasone propionate (Teva)
01 2Italy
Beclomethasone propionate (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
Beclomethasone propionate "Teva/Low"
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
11
PharmaCompass offers a list of Beclomethasone Dipropionate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, 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.
A Sanasthmyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sanasthmyl, including repackagers and relabelers. The FDA regulates Sanasthmyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sanasthmyl 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 Sanasthmyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Sanasthmyl supplier is an individual or a company that provides Sanasthmyl active pharmaceutical ingredient (API) or Sanasthmyl finished formulations upon request. The Sanasthmyl suppliers may include Sanasthmyl API manufacturers, exporters, distributors and traders.
click here to find a list of Sanasthmyl suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Sanasthmyl Drug Master File in Japan (Sanasthmyl JDMF) empowers Sanasthmyl 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 Sanasthmyl JDMF during the approval evaluation for pharmaceutical products. At the time of Sanasthmyl 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 Sanasthmyl suppliers with JDMF on PharmaCompass.
We have 1 companies offering Sanasthmyl
Get in contact with the supplier of your choice:
