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PharmaCompass offers a list of Metformin 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 Metformin manufacturer or Metformin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metformin manufacturer or Metformin supplier.
PharmaCompass also assists you with knowing the Metformin API Price utilized in the formulation of products. Metformin API Price is not always fixed or binding as the Metformin Price is obtained through a variety of data sources. The Metformin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glumetza manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glumetza, including repackagers and relabelers. The FDA regulates Glumetza manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glumetza 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 Glumetza manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glumetza supplier is an individual or a company that provides Glumetza active pharmaceutical ingredient (API) or Glumetza finished formulations upon request. The Glumetza suppliers may include Glumetza API manufacturers, exporters, distributors and traders.
click here to find a list of Glumetza 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 Glumetza Drug Master File in Japan (Glumetza JDMF) empowers Glumetza 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 Glumetza JDMF during the approval evaluation for pharmaceutical products. At the time of Glumetza 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 Glumetza suppliers with JDMF on PharmaCompass.
We have 11 companies offering Glumetza
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