01 1KUKJEON PHARMACEUTICAL Co. , Ltd.
01 1Itopride hydrochloride
01 1South Korea
Registration Number : 227MF10228
Registrant's Address : #1516, Geumgang Penterium IT Tower, 282, Hagui-ro, Dongan-gu, Anyang-si, Gyeonggi-do,...
Initial Date of Registration : 2015-09-03
Latest Date of Registration : 2015-09-03
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PharmaCompass offers a list of Itopride Hydrochloride 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 Itopride Hydrochloride manufacturer or Itopride Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Itopride Hydrochloride manufacturer or Itopride Hydrochloride supplier.
PharmaCompass also assists you with knowing the Itopride Hydrochloride API Price utilized in the formulation of products. Itopride Hydrochloride API Price is not always fixed or binding as the Itopride Hydrochloride Price is obtained through a variety of data sources. The Itopride Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ganaton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ganaton, including repackagers and relabelers. The FDA regulates Ganaton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ganaton 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 Ganaton manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ganaton supplier is an individual or a company that provides Ganaton active pharmaceutical ingredient (API) or Ganaton finished formulations upon request. The Ganaton suppliers may include Ganaton API manufacturers, exporters, distributors and traders.
click here to find a list of Ganaton 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 Ganaton Drug Master File in Japan (Ganaton JDMF) empowers Ganaton 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 Ganaton JDMF during the approval evaluation for pharmaceutical products. At the time of Ganaton 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 Ganaton suppliers with JDMF on PharmaCompass.
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