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