01 1Active Pharma Inc.
01 1Japanese Pharmacopoeia tolnaftate (production only)
01 1Japan
Japanese Pharmacopoeia Tolnaftate (for manufacturing only)
Registration Number : 217MF10195
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-08
Latest Date of Registration : 2020-06-04
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PharmaCompass offers a list of Tolnaftate 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 Tolnaftate manufacturer or Tolnaftate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tolnaftate manufacturer or Tolnaftate supplier.
PharmaCompass also assists you with knowing the Tolnaftate API Price utilized in the formulation of products. Tolnaftate API Price is not always fixed or binding as the Tolnaftate Price is obtained through a variety of data sources. The Tolnaftate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sporiline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sporiline, including repackagers and relabelers. The FDA regulates Sporiline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sporiline 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 Sporiline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sporiline supplier is an individual or a company that provides Sporiline active pharmaceutical ingredient (API) or Sporiline finished formulations upon request. The Sporiline suppliers may include Sporiline API manufacturers, exporters, distributors and traders.
click here to find a list of Sporiline 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 Sporiline Drug Master File in Japan (Sporiline JDMF) empowers Sporiline 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 Sporiline JDMF during the approval evaluation for pharmaceutical products. At the time of Sporiline 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 Sporiline suppliers with JDMF on PharmaCompass.
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