01 1ERREGIERRE S. p. A.
01 1URAAPIDIL
01 1Italy
Registration Number : 304MF10127
Registrant's Address : VIA F. BARACCA 19-24060 SAN PAOLO D'ARGON (BERGAMO) ITALY
Initial Date of Registration : 2022-08-31
Latest Date of Registration : 2022-08-31
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PharmaCompass offers a list of Urapidil 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 Urapidil Hydrochloride manufacturer or Urapidil Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Urapidil Hydrochloride manufacturer or Urapidil Hydrochloride supplier.
PharmaCompass also assists you with knowing the Urapidil Hydrochloride API Price utilized in the formulation of products. Urapidil Hydrochloride API Price is not always fixed or binding as the Urapidil Hydrochloride Price is obtained through a variety of data sources. The Urapidil Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ebrantil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ebrantil, including repackagers and relabelers. The FDA regulates Ebrantil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ebrantil 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 Ebrantil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ebrantil supplier is an individual or a company that provides Ebrantil active pharmaceutical ingredient (API) or Ebrantil finished formulations upon request. The Ebrantil suppliers may include Ebrantil API manufacturers, exporters, distributors and traders.
click here to find a list of Ebrantil 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 Ebrantil Drug Master File in Japan (Ebrantil JDMF) empowers Ebrantil 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 Ebrantil JDMF during the approval evaluation for pharmaceutical products. At the time of Ebrantil 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 Ebrantil suppliers with JDMF on PharmaCompass.
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