01 1Latina Pharma S. p. A.
01 1Aztreonam
01 1Germany
Registration Number : 219MF10225
Registrant's Address : VIA MURILLO, 7, 04013-SERMONETA (LATINA), ITALY
Initial Date of Registration : 2007-07-06
Latest Date of Registration : 2007-07-06
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PharmaCompass offers a list of Aztreonam 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 Aztreonam manufacturer or Aztreonam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aztreonam manufacturer or Aztreonam supplier.
PharmaCompass also assists you with knowing the Aztreonam API Price utilized in the formulation of products. Aztreonam API Price is not always fixed or binding as the Aztreonam Price is obtained through a variety of data sources. The Aztreonam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Azactam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azactam, including repackagers and relabelers. The FDA regulates Azactam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azactam 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 Azactam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azactam supplier is an individual or a company that provides Azactam active pharmaceutical ingredient (API) or Azactam finished formulations upon request. The Azactam suppliers may include Azactam API manufacturers, exporters, distributors and traders.
click here to find a list of Azactam 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 Azactam Drug Master File in Japan (Azactam JDMF) empowers Azactam 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 Azactam JDMF during the approval evaluation for pharmaceutical products. At the time of Azactam 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 Azactam suppliers with JDMF on PharmaCompass.
