01 1Fuji Chemical Industry Co., Ltd.
01 1Neticonazole hydrochloride (production only)
01 1Japan
Neticonazole hydrochloride (for manufacturing only)
Registration Number : 222MF10076
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2010-03-02
Latest Date of Registration : 2010-03-02
A Neticonazole Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neticonazole Hydrochloride, including repackagers and relabelers. The FDA regulates Neticonazole Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neticonazole Hydrochloride 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 Neticonazole Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Neticonazole Hydrochloride supplier is an individual or a company that provides Neticonazole Hydrochloride active pharmaceutical ingredient (API) or Neticonazole Hydrochloride finished formulations upon request. The Neticonazole Hydrochloride suppliers may include Neticonazole Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Neticonazole Hydrochloride 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 Neticonazole Hydrochloride Drug Master File in Japan (Neticonazole Hydrochloride JDMF) empowers Neticonazole Hydrochloride 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 Neticonazole Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Neticonazole Hydrochloride 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 Neticonazole Hydrochloride suppliers with JDMF on PharmaCompass.
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