01 1Lunan New Time Bio-tech Co. , Ltd.
02 2Zhejiang Ausun Pharmaceutical Co. , Ltd.
03 1Zhejiang Medicine Co. , Ltd. Xinchang Pharmaceutical Factory
01 4Miglitol
01 4China
Registration Number : 228MF10006
Registrant's Address : No. 1, North Outer Ring Road, Feixian County, Shandong Province, China
Initial Date of Registration : 2016-01-08
Latest Date of Registration : 2020-08-05
Registration Number : 305MF10034
Registrant's Address : No. 5, Donghai 4th Avenue, Zhejiang Chemical Materials Base Linhai Zone, Zhejiang, Ch...
Initial Date of Registration : 2023-03-15
Latest Date of Registration : 2023-03-15
Registration Number : 228MF10052
Registrant's Address : No. 5, Donghai 4th Avenue, Zhejiang Chemical Materials Base Linhai Zone, Zhejiang, Ch...
Initial Date of Registration : 2016-02-18
Latest Date of Registration : 2016-02-18
Registration Number : 227MF10281
Registrant's Address : 59 East Huancheng Road, Xinchang, Zhejiang, P. R. China
Initial Date of Registration : 2015-12-15
Latest Date of Registration : 2019-01-24
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PharmaCompass offers a list of Miglitol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Miglitol manufacturer or Miglitol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Miglitol manufacturer or Miglitol supplier.
PharmaCompass also assists you with knowing the Miglitol API Price utilized in the formulation of products. Miglitol API Price is not always fixed or binding as the Miglitol Price is obtained through a variety of data sources. The Miglitol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glyset manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glyset, including repackagers and relabelers. The FDA regulates Glyset manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glyset 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 Glyset manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glyset supplier is an individual or a company that provides Glyset active pharmaceutical ingredient (API) or Glyset finished formulations upon request. The Glyset suppliers may include Glyset API manufacturers, exporters, distributors and traders.
click here to find a list of Glyset 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 Glyset Drug Master File in Japan (Glyset JDMF) empowers Glyset 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 Glyset JDMF during the approval evaluation for pharmaceutical products. At the time of Glyset 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 Glyset suppliers with JDMF on PharmaCompass.
We have 3 companies offering Glyset
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