01 1Shiratori Pharmaceutical Co., Ltd.
01 1Pimobendan production dedicated
01 1Japan
Pimo Bendan (for manufacturing purposes only)
Registration Number : 218MF10997
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2006-12-18
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PharmaCompass offers a list of Pimobendan 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 Pimobendan manufacturer or Pimobendan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pimobendan manufacturer or Pimobendan supplier.
PharmaCompass also assists you with knowing the Pimobendan API Price utilized in the formulation of products. Pimobendan API Price is not always fixed or binding as the Pimobendan Price is obtained through a variety of data sources. The Pimobendan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acardi manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acardi, including repackagers and relabelers. The FDA regulates Acardi manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acardi 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 Acardi manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acardi supplier is an individual or a company that provides Acardi active pharmaceutical ingredient (API) or Acardi finished formulations upon request. The Acardi suppliers may include Acardi API manufacturers, exporters, distributors and traders.
click here to find a list of Acardi 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 Acardi Drug Master File in Japan (Acardi JDMF) empowers Acardi 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 Acardi JDMF during the approval evaluation for pharmaceutical products. At the time of Acardi 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 Acardi suppliers with JDMF on PharmaCompass.
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