01 1Active Pharma Co., Ltd.
01 1Japanese Pharmacopoeia tolnaftate (production only)
01 1Japan
Japanese Pharmacopoeia Tolnaftate (for manufacturing purposes 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.
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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 Chinosol Brand of Tolnaftate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chinosol Brand of Tolnaftate, including repackagers and relabelers. The FDA regulates Chinosol Brand of Tolnaftate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chinosol Brand of Tolnaftate 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 Chinosol Brand of Tolnaftate supplier is an individual or a company that provides Chinosol Brand of Tolnaftate active pharmaceutical ingredient (API) or Chinosol Brand of Tolnaftate finished formulations upon request. The Chinosol Brand of Tolnaftate suppliers may include Chinosol Brand of Tolnaftate API manufacturers, exporters, distributors and traders.
click here to find a list of Chinosol Brand of Tolnaftate 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 Chinosol Brand of Tolnaftate Drug Master File in Japan (Chinosol Brand of Tolnaftate JDMF) empowers Chinosol Brand of Tolnaftate 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 Chinosol Brand of Tolnaftate JDMF during the approval evaluation for pharmaceutical products. At the time of Chinosol Brand of Tolnaftate 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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