01 1Daito Co., Ltd.
01 1Day stations pindolol (production only)
01 1Japan
JP Pindolol (for manufacturing purposes only)
Registration Number : 217MF10627
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-09-29
Latest Date of Registration : 2006-08-23
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PharmaCompass offers a list of Pindolol 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 Pindolol manufacturer or Pindolol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pindolol manufacturer or Pindolol supplier.
PharmaCompass also assists you with knowing the Pindolol API Price utilized in the formulation of products. Pindolol API Price is not always fixed or binding as the Pindolol Price is obtained through a variety of data sources. The Pindolol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glauco-Viskin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glauco-Viskin, including repackagers and relabelers. The FDA regulates Glauco-Viskin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glauco-Viskin 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 Glauco-Viskin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glauco-Viskin supplier is an individual or a company that provides Glauco-Viskin active pharmaceutical ingredient (API) or Glauco-Viskin finished formulations upon request. The Glauco-Viskin suppliers may include Glauco-Viskin API manufacturers, exporters, distributors and traders.
click here to find a list of Glauco-Viskin 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 Glauco-Viskin Drug Master File in Japan (Glauco-Viskin JDMF) empowers Glauco-Viskin 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 Glauco-Viskin JDMF during the approval evaluation for pharmaceutical products. At the time of Glauco-Viskin 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 Glauco-Viskin suppliers with JDMF on PharmaCompass.
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