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01 1Corden Pharma Bergamo S. p. A.
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01 1METRONIDAZOLE
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01 1Italy
Registration Number : 220MF10104
Registrant's Address : Via Bergamo, 121, I-24047, TREVIGLIO (Bg), Italy
Initial Date of Registration : 2008-04-11
Latest Date of Registration : 2015-11-12
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PharmaCompass offers a list of Metronidazole 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 Metronidazole manufacturer or Metronidazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metronidazole manufacturer or Metronidazole supplier.
PharmaCompass also assists you with knowing the Metronidazole API Price utilized in the formulation of products. Metronidazole API Price is not always fixed or binding as the Metronidazole Price is obtained through a variety of data sources. The Metronidazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Arilin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arilin, including repackagers and relabelers. The FDA regulates Arilin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arilin 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 Arilin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Arilin supplier is an individual or a company that provides Arilin active pharmaceutical ingredient (API) or Arilin finished formulations upon request. The Arilin suppliers may include Arilin API manufacturers, exporters, distributors and traders.
click here to find a list of Arilin 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 Arilin Drug Master File in Japan (Arilin JDMF) empowers Arilin 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 Arilin JDMF during the approval evaluation for pharmaceutical products. At the time of Arilin 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 Arilin suppliers with JDMF on PharmaCompass.
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