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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 Itopride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Itopride, including repackagers and relabelers. The FDA regulates Itopride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Itopride 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 Itopride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Itopride supplier is an individual or a company that provides Itopride active pharmaceutical ingredient (API) or Itopride finished formulations upon request. The Itopride suppliers may include Itopride API manufacturers, exporters, distributors and traders.
click here to find a list of Itopride 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 Itopride Drug Master File in Japan (Itopride JDMF) empowers Itopride 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 Itopride JDMF during the approval evaluation for pharmaceutical products. At the time of Itopride 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 Itopride suppliers with JDMF on PharmaCompass.
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