01 1ERREGIERRE S. p. A.
01 1Nitrate oxiconazole
01 1Italy
Registration Number : 220MF10204
Registrant's Address : VIA F. BARACCA 19-24060 SAN PAOLO D'ARGON (BERGAMO) ITALY
Initial Date of Registration : 2008-09-29
Latest Date of Registration : 2008-09-29
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PharmaCompass offers a list of Oxiconazole Nitrate 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 Oxiconazole Nitrate manufacturer or Oxiconazole Nitrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxiconazole Nitrate manufacturer or Oxiconazole Nitrate supplier.
PharmaCompass also assists you with knowing the Oxiconazole Nitrate API Price utilized in the formulation of products. Oxiconazole Nitrate API Price is not always fixed or binding as the Oxiconazole Nitrate Price is obtained through a variety of data sources. The Oxiconazole Nitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Myfungar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Myfungar, including repackagers and relabelers. The FDA regulates Myfungar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Myfungar 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 Myfungar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Myfungar supplier is an individual or a company that provides Myfungar active pharmaceutical ingredient (API) or Myfungar finished formulations upon request. The Myfungar suppliers may include Myfungar API manufacturers, exporters, distributors and traders.
click here to find a list of Myfungar 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 Myfungar Drug Master File in Japan (Myfungar JDMF) empowers Myfungar 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 Myfungar JDMF during the approval evaluation for pharmaceutical products. At the time of Myfungar 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 Myfungar suppliers with JDMF on PharmaCompass.
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