01 1Shiono Finesse Co., Ltd.
01 1Isoproterenol hydrochloride
01 1Japan
Registration Number : 220MF10065
Registrant's Address : 3-1-6 Doshomachi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2008-02-25
Latest Date of Registration : 2008-02-25
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PharmaCompass offers a list of Isoproterenol 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 Isoproterenol Hydrochloride manufacturer or Isoproterenol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isoproterenol Hydrochloride manufacturer or Isoproterenol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Isoproterenol Hydrochloride API Price utilized in the formulation of products. Isoproterenol Hydrochloride API Price is not always fixed or binding as the Isoproterenol Hydrochloride Price is obtained through a variety of data sources. The Isoproterenol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Medihaler-ISO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Medihaler-ISO, including repackagers and relabelers. The FDA regulates Medihaler-ISO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Medihaler-ISO 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 Medihaler-ISO manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Medihaler-ISO supplier is an individual or a company that provides Medihaler-ISO active pharmaceutical ingredient (API) or Medihaler-ISO finished formulations upon request. The Medihaler-ISO suppliers may include Medihaler-ISO API manufacturers, exporters, distributors and traders.
click here to find a list of Medihaler-ISO 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 Medihaler-ISO Drug Master File in Japan (Medihaler-ISO JDMF) empowers Medihaler-ISO 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 Medihaler-ISO JDMF during the approval evaluation for pharmaceutical products. At the time of Medihaler-ISO 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 Medihaler-ISO suppliers with JDMF on PharmaCompass.
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