01 1ACS DOBFAR S. p. A.
02 1Eumedica Pharmaceuticals Industries
03 1Jiangxi Fushine Pharmaceutical Co. , Ltd.
04 2Kyongbo Pharmaceutical Co. , Ltd.
05 2North China Pharmaceutical Group Semisyntech Co. , Ltd.
06 1Shin Poong Pharm. Co. , Ltd.
07 1Sichuan Renan Pharmaceutical Co. , Ltd.
01 1Japanese Pharmacopoeia sulbactam sodium (production only)
02 1SULBACTAM SODIUM
03 1Sulbactam Sodium
04 4Sulbactam sodium
05 1Sulbactam sodium (production only)
06 1Sulbactam sodium (sterile)
01 4China
02 1Italy
03 3South Korea
04 1Spain
Registration Number : 228MF10054
Registrant's Address : Viale Addetta, 4/12, 20067 Tribiano (Milan) Italy
Initial Date of Registration : 2016-02-18
Latest Date of Registration : 2024-02-07
Registration Number : 220MF10060
Registrant's Address : Poligono Industrial de Silvota, parcelas 22B-23 E-33192 Silvota, Llanera-Asturias (Sp...
Initial Date of Registration : 2008-02-25
Latest Date of Registration : 2021-07-09
Registration Number : 227MF10104
Registrant's Address : No. 2 Yuli Industrial Zone, Changjiang District, Jingdezhen City 333000, Jiangxi, Chi...
Initial Date of Registration : 2015-04-09
Latest Date of Registration : 2023-04-12
Sulbactam Sodium (for manufacturing only)
Registration Number : 219MF10293
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2007-09-10
Latest Date of Registration : 2019-03-29
Japanese Pharmacopoeia Sulbactam Sodium (for manufacturing only)
Registration Number : 218MF10710
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2006-08-14
Latest Date of Registration : 2019-03-29
Registration Number : 226MF10212
Registrant's Address : No. 20 Yangzi Road, Shijiazhuang Economic and Technological Development Zone, Hebei 0...
Initial Date of Registration : 2014-11-17
Latest Date of Registration : 2014-11-17
Registration Number : 230MF10001
Registrant's Address : No. 20 Yangzi Road, Shijiazhuang Economic and Technological Development Zone, Hebei 0...
Initial Date of Registration : 2018-01-10
Latest Date of Registration : 2018-01-10
Registration Number : 229MF10066
Registrant's Address : 161, Yeoksam-ro, Gangnam-gu, Seoul, Korea
Initial Date of Registration : 2017-03-17
Latest Date of Registration : 2017-07-31
Registration Number : 303MF10153
Registrant's Address : No. 9, Ren'an section, Health Road, Jiulong Town (Industrial Park) Yuechi, Sichuan.
Initial Date of Registration : 2021-09-28
Latest Date of Registration : 2021-09-28
A Sulbactam Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulbactam Sodium, including repackagers and relabelers. The FDA regulates Sulbactam Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulbactam 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 Sulbactam Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sulbactam Sodium supplier is an individual or a company that provides Sulbactam Sodium active pharmaceutical ingredient (API) or Sulbactam Sodium finished formulations upon request. The Sulbactam Sodium suppliers may include Sulbactam Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Sulbactam 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 Sulbactam Sodium Drug Master File in Japan (Sulbactam Sodium JDMF) empowers Sulbactam 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 Sulbactam Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Sulbactam 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 Sulbactam Sodium suppliers with JDMF on PharmaCompass.
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