01 2Oryza Oil & Fat Chemical Co., Ltd.
01 2Japanese Pharmacopoeia Acrinol
01 2Japan
Acrinol, Japanese Pharmacopoeia
Registration Number : 224MF10045
Registrant's Address : 1 Numata, Kitakata, Kitakata-cho, Ichinomiya City, Aichi Prefecture
Initial Date of Registration : 2012-02-28
Latest Date of Registration : 2012-02-28
Acrinol, Japanese Pharmacopoeia
Registration Number : 218MF10807
Registrant's Address : 1 Numata, Kitakata, Kitakata-cho, Ichinomiya City, Aichi Prefecture
Initial Date of Registration : 2006-10-06
Latest Date of Registration : 2010-11-29
A Ethacridine Lactate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethacridine Lactate, including repackagers and relabelers. The FDA regulates Ethacridine Lactate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethacridine Lactate 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 Ethacridine Lactate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethacridine Lactate supplier is an individual or a company that provides Ethacridine Lactate active pharmaceutical ingredient (API) or Ethacridine Lactate finished formulations upon request. The Ethacridine Lactate suppliers may include Ethacridine Lactate API manufacturers, exporters, distributors and traders.
click here to find a list of Ethacridine Lactate 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 Ethacridine Lactate Drug Master File in Japan (Ethacridine Lactate JDMF) empowers Ethacridine Lactate 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 Ethacridine Lactate JDMF during the approval evaluation for pharmaceutical products. At the time of Ethacridine Lactate 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 Ethacridine Lactate suppliers with JDMF on PharmaCompass.
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