Axplora- The partner of choice for complex APIs.
01 1Farmabios S. p. A.
02 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Amcinonide
02 1Amcinonide "Teva"
01 1Germany
02 1Italy
Axplora- The partner of choice for complex APIs.
Registration Number : 305MF10048
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2023-04-12
Latest Date of Registration : 2023-04-12
Registration Number : 218MF10911
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
A Amcinonide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amcinonide, including repackagers and relabelers. The FDA regulates Amcinonide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amcinonide 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 Amcinonide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amcinonide supplier is an individual or a company that provides Amcinonide active pharmaceutical ingredient (API) or Amcinonide finished formulations upon request. The Amcinonide suppliers may include Amcinonide API manufacturers, exporters, distributors and traders.
click here to find a list of Amcinonide 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 Amcinonide Drug Master File in Japan (Amcinonide JDMF) empowers Amcinonide 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 Amcinonide JDMF during the approval evaluation for pharmaceutical products. At the time of Amcinonide 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 Amcinonide suppliers with JDMF on PharmaCompass.
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