01 1Active Pharma Co., Ltd.
01 1Japanese Pharmacopoeia tolnaftate (production only)
01 1Japan
Japanese Pharmacopoeia Tornaftate (for manufacturing purposes only)
Registration Number : 217MF10195
Registrant's Address : 2-36-1 Kanda Jimbocho, 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, and more, enabling you to easily find the right Tolnaftate manufacturer or Tolnaftate supplier for your needs.
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A Tineafax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tineafax, including repackagers and relabelers. The FDA regulates Tineafax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tineafax 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 Tineafax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Tineafax supplier is an individual or a company that provides Tineafax active pharmaceutical ingredient (API) or Tineafax finished formulations upon request. The Tineafax suppliers may include Tineafax API manufacturers, exporters, distributors and traders.
click here to find a list of Tineafax suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Tineafax Drug Master File in Japan (Tineafax JDMF) empowers Tineafax 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 Tineafax JDMF during the approval evaluation for pharmaceutical products. At the time of Tineafax 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 Tineafax suppliers with JDMF on PharmaCompass.
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