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.
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 ZINC00057522 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZINC00057522, including repackagers and relabelers. The FDA regulates ZINC00057522 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZINC00057522 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 ZINC00057522 supplier is an individual or a company that provides ZINC00057522 active pharmaceutical ingredient (API) or ZINC00057522 finished formulations upon request. The ZINC00057522 suppliers may include ZINC00057522 API manufacturers, exporters, distributors and traders.
click here to find a list of ZINC00057522 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 ZINC00057522 Drug Master File in Japan (ZINC00057522 JDMF) empowers ZINC00057522 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 ZINC00057522 JDMF during the approval evaluation for pharmaceutical products. At the time of ZINC00057522 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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