Registration Number : 230MF10011
Registrant's Address : 6-2-10 Ginza, Chuo-ku, Tokyo
Initial Date of Registration : 2018-01-24
Latest Date of Registration : 2018-01-24
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PharmaCompass offers a list of Penicillin V 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 Penicillin V manufacturer or Penicillin V supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Penicillin V manufacturer or Penicillin V supplier.
PharmaCompass also assists you with knowing the Penicillin V API Price utilized in the formulation of products. Penicillin V API Price is not always fixed or binding as the Penicillin V Price is obtained through a variety of data sources. The Penicillin V Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Veetids manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Veetids, including repackagers and relabelers. The FDA regulates Veetids manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Veetids 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 Veetids manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Veetids supplier is an individual or a company that provides Veetids active pharmaceutical ingredient (API) or Veetids finished formulations upon request. The Veetids suppliers may include Veetids API manufacturers, exporters, distributors and traders.
click here to find a list of Veetids 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 Veetids Drug Master File in Japan (Veetids JDMF) empowers Veetids 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 Veetids JDMF during the approval evaluation for pharmaceutical products. At the time of Veetids 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 Veetids suppliers with JDMF on PharmaCompass.
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