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