01 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
02 1Fuji Chemical Industry Co., Ltd.
03 1Shiono Finesse Co., Ltd.
04 1UBE Co., Ltd.
05 1Zhejiang Tianyu Pharmaceutical Co. , Ltd.
01 3Silodosin
02 1Silodosin
03 1Silodosin (production only)
01 1China
02 3Japan
03 1South Korea
Registration Number : 230MF10008
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Manse-gu, Hwaseong-si, Gyeonggi-do, Republic of...
Initial Date of Registration : 2018-01-18
Latest Date of Registration : 2023-10-12
Silodosin (for manufacturing purposes only)
Registration Number : 229MF10126
Registrant's Address : 55 Yokohoonji, Kamiichi-machi, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2017-07-14
Latest Date of Registration : 2017-07-14
Registration Number : 229MF10119
Registrant's Address : 3-1-6 Doshomachi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2017-07-10
Latest Date of Registration : 2017-07-10
Registration Number : 230MF10002
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2018-01-10
Latest Date of Registration : 2018-01-10
Silodosin "For manufacturing purposes only"
Registration Number : 230MF10036
Registrant's Address : Jiangkou Development Zone, Huangyan, Taizhou City, Zhejiang Province, People's Republ...
Initial Date of Registration : 2018-02-26
Latest Date of Registration : 2018-02-26
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PharmaCompass offers a list of Silodosin 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 Silodosin manufacturer or Silodosin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Silodosin manufacturer or Silodosin supplier.
A KAD-3213, KMD-3213 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KAD-3213, KMD-3213, including repackagers and relabelers. The FDA regulates KAD-3213, KMD-3213 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KAD-3213, KMD-3213 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 KAD-3213, KMD-3213 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A KAD-3213, KMD-3213 supplier is an individual or a company that provides KAD-3213, KMD-3213 active pharmaceutical ingredient (API) or KAD-3213, KMD-3213 finished formulations upon request. The KAD-3213, KMD-3213 suppliers may include KAD-3213, KMD-3213 API manufacturers, exporters, distributors and traders.
click here to find a list of KAD-3213, KMD-3213 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 KAD-3213, KMD-3213 Drug Master File in Japan (KAD-3213, KMD-3213 JDMF) empowers KAD-3213, KMD-3213 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 KAD-3213, KMD-3213 JDMF during the approval evaluation for pharmaceutical products. At the time of KAD-3213, KMD-3213 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 KAD-3213, KMD-3213 suppliers with JDMF on PharmaCompass.
We have 5 companies offering KAD-3213, KMD-3213
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