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