01 1CKD Bio Corporation
02 1CSPC Shengxue Glucose Co. , Ltd.
03 1Zhejiang Hisun Pharmaceutical Co. , Ltd.
01 3Acarbose
01 2China
02 1South Korea
Registration Number : 220MF10038
Registrant's Address : 8, Chungjeong-ro, Seodaemun-gu, Seoul, Republic of Korea
Initial Date of Registration : 2008-02-05
Latest Date of Registration : 2008-02-05
Registration Number : 303MF10047
Registrant's Address : No. 48 Shengxue Road, Luncheng District, Shijiazhuang City, Hebei Province, China
Initial Date of Registration : 2021-03-17
Latest Date of Registration : 2021-03-17
Registration Number : 218MF10411
Registrant's Address : 46 Waisha Road, Jiaojiang District, Taizhou City, Zhejiang Province, P. R. China 3180...
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2007-01-17
A Acarbose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acarbose, including repackagers and relabelers. The FDA regulates Acarbose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acarbose 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 Acarbose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acarbose supplier is an individual or a company that provides Acarbose active pharmaceutical ingredient (API) or Acarbose finished formulations upon request. The Acarbose suppliers may include Acarbose API manufacturers, exporters, distributors and traders.
click here to find a list of Acarbose 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 Acarbose Drug Master File in Japan (Acarbose JDMF) empowers Acarbose 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 Acarbose JDMF during the approval evaluation for pharmaceutical products. At the time of Acarbose 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 Acarbose suppliers with JDMF on PharmaCompass.
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