01 1Kyongbo Pharmaceutical Co. , Ltd.
02 1Yamasa Soy Sauce Co., Ltd.
01 1Axis Aho Sol sodium
02 1Diquafosol Sodium
01 1Japan
02 1South Korea
Registration Number : 304MF10089
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2022-06-22
Latest Date of Registration : 2022-06-22
Registration Number : 220MF10109
Registrant's Address : 2-10-1 Shinseicho, Choshi City, Chiba Prefecture
Initial Date of Registration : 2008-04-11
Latest Date of Registration : 2022-05-06
A Diquafosol Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diquafosol Sodium, including repackagers and relabelers. The FDA regulates Diquafosol Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diquafosol Sodium 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 Diquafosol Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diquafosol Sodium supplier is an individual or a company that provides Diquafosol Sodium active pharmaceutical ingredient (API) or Diquafosol Sodium finished formulations upon request. The Diquafosol Sodium suppliers may include Diquafosol Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Diquafosol Sodium 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 Diquafosol Sodium Drug Master File in Japan (Diquafosol Sodium JDMF) empowers Diquafosol Sodium 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 Diquafosol Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Diquafosol Sodium 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 Diquafosol Sodium suppliers with JDMF on PharmaCompass.
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