01 1Yatsushiro Pharmaceutical Co., Ltd.
01 1Aminophylline hydrate
01 1Blank
Registration Number : 222MF10082
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2010-03-09
Latest Date of Registration : 2010-03-09
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PharmaCompass offers a list of Aminophylline 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 Aminophylline manufacturer or Aminophylline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aminophylline manufacturer or Aminophylline supplier.
PharmaCompass also assists you with knowing the Aminophylline API Price utilized in the formulation of products. Aminophylline API Price is not always fixed or binding as the Aminophylline Price is obtained through a variety of data sources. The Aminophylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eufilina Venosa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eufilina Venosa, including repackagers and relabelers. The FDA regulates Eufilina Venosa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eufilina Venosa API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Eufilina Venosa supplier is an individual or a company that provides Eufilina Venosa active pharmaceutical ingredient (API) or Eufilina Venosa finished formulations upon request. The Eufilina Venosa suppliers may include Eufilina Venosa API manufacturers, exporters, distributors and traders.
click here to find a list of Eufilina Venosa 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 Eufilina Venosa Drug Master File in Japan (Eufilina Venosa JDMF) empowers Eufilina Venosa 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 Eufilina Venosa JDMF during the approval evaluation for pharmaceutical products. At the time of Eufilina Venosa 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 Eufilina Venosa suppliers with JDMF on PharmaCompass.
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