01 1Bal Pharma Limited
02 1Edmond Pharma s. r. l.
03 1Ohara Pharmaceutical Co., Ltd.
04 1Oril Industry
05 3Zhejiang Jiuzhou Pharmaceutical Co. , Ltd.
01 1GLICLAZIDE
02 5Gliclazide
03 1Japanese Pharmacopoeia gliclazide (production only)
01 3China
02 1France
03 1India
04 1Japan
05 1Sweden
Registration Number : 220MF10140
Registrant's Address : 5th Floor, Lakshminarayan Complex, 10/1, Palace Road, Bangalore-560052, India
Initial Date of Registration : 2008-06-10
Latest Date of Registration : 2008-06-10
Japanese Pharmacopoeia Gliclazide (for manufacturing purposes only)
Registration Number : 226MF10188
Registrant's Address : 121-15 Torino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2014-09-30
Latest Date of Registration : 2014-09-30
Registration Number : 221MF10193
Registrant's Address : Via G. B. Grassi 15-20157 Milano Italy
Initial Date of Registration : 2009-08-31
Latest Date of Registration : 2009-08-31
Registration Number : 217MF10332
Registrant's Address : 13, rue Auguste Desgene(') tais, 76210 Bolbec, FRANCE
Initial Date of Registration : 2005-08-09
Latest Date of Registration : 2018-04-09
Registration Number : 227MF10100
Registrant's Address : Waisha Road 99# Jiaojiang Taizhou City, Zhejiang China
Initial Date of Registration : 2015-04-09
Latest Date of Registration : 2021-07-28
Registration Number : 224MF10097
Registrant's Address : Waisha Road 99# Jiaojiang District Taizhou City Zhejiang Province China
Initial Date of Registration : 2012-05-08
Latest Date of Registration : 2012-05-08
Registration Number : 221MF10162
Registrant's Address : Waisha Road 99# Jiaojiang Taizhou City Zhejiang China
Initial Date of Registration : 2009-07-23
Latest Date of Registration : 2009-07-23
54
PharmaCompass offers a list of Gliclazide 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 Gliclazide manufacturer or Gliclazide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gliclazide manufacturer or Gliclazide supplier.
PharmaCompass also assists you with knowing the Gliclazide API Price utilized in the formulation of products. Gliclazide API Price is not always fixed or binding as the Gliclazide Price is obtained through a variety of data sources. The Gliclazide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diamicron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diamicron, including repackagers and relabelers. The FDA regulates Diamicron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diamicron 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 Diamicron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diamicron supplier is an individual or a company that provides Diamicron active pharmaceutical ingredient (API) or Diamicron finished formulations upon request. The Diamicron suppliers may include Diamicron API manufacturers, exporters, distributors and traders.
click here to find a list of Diamicron 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 Diamicron Drug Master File in Japan (Diamicron JDMF) empowers Diamicron 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 Diamicron JDMF during the approval evaluation for pharmaceutical products. At the time of Diamicron 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 Diamicron suppliers with JDMF on PharmaCompass.
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