01 1Ace Japan Co., Ltd.
02 1Juzen Chemical Co., Ltd.
03 2NAKODA CHEMICALS LIMITED
01 1Ecabet sodium
02 1Ecabet sodium (N)
03 1Ecabet sodium (Shiquan)
04 1Ecabet sodium hydrate
01 2India
02 2Japan
Registration Number : 226MF10134
Registrant's Address : 5850-1 Higashine-ko, Higashine City, Yamagata Prefecture
Initial Date of Registration : 2014-07-02
Latest Date of Registration : 2014-07-02
Registration Number : 217MF10010
Registrant's Address : 1-10 Kibacho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-05-18
Latest Date of Registration : 2006-11-15
Registration Number : 218MF10769
Registrant's Address : D-9 SMR NIRANJAN JUPITOR COLONY SIKH ROAD SECUNDERABAD INDIA
Initial Date of Registration : 2006-09-22
Latest Date of Registration : 2006-09-22
Registration Number : 226MF10089
Registrant's Address : Plot No. 64/A & 65/B, Phase-I, IDA, Jeedimetla, Hyderabad-500 055, Telangana State, I...
Initial Date of Registration : 2014-05-09
Latest Date of Registration : 2014-05-09
A Ecabet Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ecabet Sodium, including repackagers and relabelers. The FDA regulates Ecabet Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ecabet 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 Ecabet Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ecabet Sodium supplier is an individual or a company that provides Ecabet Sodium active pharmaceutical ingredient (API) or Ecabet Sodium finished formulations upon request. The Ecabet Sodium suppliers may include Ecabet Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Ecabet 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 Ecabet Sodium Drug Master File in Japan (Ecabet Sodium JDMF) empowers Ecabet 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 Ecabet Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Ecabet 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 Ecabet Sodium suppliers with JDMF on PharmaCompass.
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