01 1Quimica Syntetica S. A.
01 1Guanfacine hydrochloride
01 1Spain
Registration Number : 227MF10293
Registrant's Address : Calle Dulcinea, s/n 28805 Alcala De Henares Madrid Spain
Initial Date of Registration : 2015-12-24
Latest Date of Registration : 2017-01-31
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PharmaCompass offers a list of Guanfacine 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 Guanfacine manufacturer or Guanfacine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Guanfacine manufacturer or Guanfacine supplier.
PharmaCompass also assists you with knowing the Guanfacine API Price utilized in the formulation of products. Guanfacine API Price is not always fixed or binding as the Guanfacine Price is obtained through a variety of data sources. The Guanfacine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Estulic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estulic, including repackagers and relabelers. The FDA regulates Estulic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estulic 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 Estulic manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Estulic supplier is an individual or a company that provides Estulic active pharmaceutical ingredient (API) or Estulic finished formulations upon request. The Estulic suppliers may include Estulic API manufacturers, exporters, distributors and traders.
click here to find a list of Estulic 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 Estulic Drug Master File in Japan (Estulic JDMF) empowers Estulic 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 Estulic JDMF during the approval evaluation for pharmaceutical products. At the time of Estulic 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 Estulic suppliers with JDMF on PharmaCompass.
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