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PharmaCompass offers a list of Pranlukast 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 Pranlukast manufacturer or Pranlukast supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pranlukast manufacturer or Pranlukast supplier.
PharmaCompass also assists you with knowing the Pranlukast API Price utilized in the formulation of products. Pranlukast API Price is not always fixed or binding as the Pranlukast Price is obtained through a variety of data sources. The Pranlukast Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pranlukast Hemihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pranlukast Hemihydrate, including repackagers and relabelers. The FDA regulates Pranlukast Hemihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pranlukast Hemihydrate 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 Pranlukast Hemihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pranlukast Hemihydrate supplier is an individual or a company that provides Pranlukast Hemihydrate active pharmaceutical ingredient (API) or Pranlukast Hemihydrate finished formulations upon request. The Pranlukast Hemihydrate suppliers may include Pranlukast Hemihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Pranlukast Hemihydrate 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 Pranlukast Hemihydrate Drug Master File in Japan (Pranlukast Hemihydrate JDMF) empowers Pranlukast Hemihydrate 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 Pranlukast Hemihydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Pranlukast Hemihydrate 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 Pranlukast Hemihydrate suppliers with JDMF on PharmaCompass.
We have 13 companies offering Pranlukast Hemihydrate
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Market Place
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
