01 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Diflorasone acetic acid ester "Teva"
01 1Italy
Registration Number : 218MF10899
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 Diflorasone 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 Diflorasone manufacturer or Diflorasone supplier for your needs.
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PharmaCompass also assists you with knowing the Diflorasone API Price utilized in the formulation of products. Diflorasone API Price is not always fixed or binding as the Diflorasone Price is obtained through a variety of data sources. The Diflorasone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prestwick3_000619 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000619, including repackagers and relabelers. The FDA regulates Prestwick3_000619 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000619 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 Prestwick3_000619 supplier is an individual or a company that provides Prestwick3_000619 active pharmaceutical ingredient (API) or Prestwick3_000619 finished formulations upon request. The Prestwick3_000619 suppliers may include Prestwick3_000619 API manufacturers, exporters, distributors and traders.
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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 Prestwick3_000619 Drug Master File in Japan (Prestwick3_000619 JDMF) empowers Prestwick3_000619 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 Prestwick3_000619 JDMF during the approval evaluation for pharmaceutical products. At the time of Prestwick3_000619 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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