01 1Novartis Pharmaceutical Manufacturing LLC
01 1Lithium carbonate
01 1Slovenia
Registration Number : 217MF10493
Registrant's Address : Verovskova ulica 57, 1000 Ljubljana, Slovenia
Initial Date of Registration : 2005-09-06
Latest Date of Registration : 2007-05-15
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PharmaCompass offers a list of Lithium Carbonate 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 Lithium Carbonate manufacturer or Lithium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lithium Carbonate manufacturer or Lithium Carbonate supplier.
PharmaCompass also assists you with knowing the Lithium Carbonate API Price utilized in the formulation of products. Lithium Carbonate API Price is not always fixed or binding as the Lithium Carbonate Price is obtained through a variety of data sources. The Lithium Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Duralite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duralite, including repackagers and relabelers. The FDA regulates Duralite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duralite 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 Duralite manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duralite supplier is an individual or a company that provides Duralite active pharmaceutical ingredient (API) or Duralite finished formulations upon request. The Duralite suppliers may include Duralite API manufacturers, exporters, distributors and traders.
click here to find a list of Duralite 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 Duralite Drug Master File in Japan (Duralite JDMF) empowers Duralite 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 Duralite JDMF during the approval evaluation for pharmaceutical products. At the time of Duralite 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 Duralite suppliers with JDMF on PharmaCompass.
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