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 Dermoxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dermoxin, including repackagers and relabelers. The FDA regulates Dermoxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dermoxin 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 Dermoxin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dermoxin supplier is an individual or a company that provides Dermoxin active pharmaceutical ingredient (API) or Dermoxin finished formulations upon request. The Dermoxin suppliers may include Dermoxin API manufacturers, exporters, distributors and traders.
click here to find a list of Dermoxin 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 Dermoxin Drug Master File in Japan (Dermoxin JDMF) empowers Dermoxin 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 Dermoxin JDMF during the approval evaluation for pharmaceutical products. At the time of Dermoxin 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 Dermoxin suppliers with JDMF on PharmaCompass.
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