Registration Number : 217MF10889
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2005-11-07
Latest Date of Registration : 2008-03-14
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PharmaCompass offers a list of Furazolidone 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 Furazolidone manufacturer or Furazolidone supplier for your needs.
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A Furox Aerosol Powder (Veterinary) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Furox Aerosol Powder (Veterinary), including repackagers and relabelers. The FDA regulates Furox Aerosol Powder (Veterinary) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Furox Aerosol Powder (Veterinary) 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 Furox Aerosol Powder (Veterinary) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Furox Aerosol Powder (Veterinary) supplier is an individual or a company that provides Furox Aerosol Powder (Veterinary) active pharmaceutical ingredient (API) or Furox Aerosol Powder (Veterinary) finished formulations upon request. The Furox Aerosol Powder (Veterinary) suppliers may include Furox Aerosol Powder (Veterinary) API manufacturers, exporters, distributors and traders.
click here to find a list of Furox Aerosol Powder (Veterinary) 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 Furox Aerosol Powder (Veterinary) Drug Master File in Japan (Furox Aerosol Powder (Veterinary) JDMF) empowers Furox Aerosol Powder (Veterinary) 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 Furox Aerosol Powder (Veterinary) JDMF during the approval evaluation for pharmaceutical products. At the time of Furox Aerosol Powder (Veterinary) 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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