01 1Cambrex Profarmaco Milano S. r. l.
02 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Adrenalin
02 1Epinephrine
01 1Taiwan
02 1U.S.A
Registration Number : 226MF10196
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2014-10-27
Latest Date of Registration : 2020-04-22
Registration Number : 230MF10047
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2018-03-27
Latest Date of Registration : 2018-03-27
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PharmaCompass offers a list of Epinephrine 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 Epinephrine manufacturer or Epinephrine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Epinephrine manufacturer or Epinephrine supplier.
PharmaCompass also assists you with knowing the Epinephrine API Price utilized in the formulation of products. Epinephrine API Price is not always fixed or binding as the Epinephrine Price is obtained through a variety of data sources. The Epinephrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Suprel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Suprel, including repackagers and relabelers. The FDA regulates Suprel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Suprel 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 Suprel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Suprel supplier is an individual or a company that provides Suprel active pharmaceutical ingredient (API) or Suprel finished formulations upon request. The Suprel suppliers may include Suprel API manufacturers, exporters, distributors and traders.
click here to find a list of Suprel 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 Suprel Drug Master File in Japan (Suprel JDMF) empowers Suprel 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 Suprel JDMF during the approval evaluation for pharmaceutical products. At the time of Suprel 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 Suprel suppliers with JDMF on PharmaCompass.
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