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01 Kongo Chemical Co., Ltd. (2)
01 Chlorpheniramine maleate (manufactured only) (1)
02 d- chlorpheniramine maleate (manufactured only) (1)
01 Japan (2)
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PharmaCompass offers a list of Chlorpheniramine Maleate 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 Chlorpheniramine Maleate manufacturer or Chlorpheniramine Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorpheniramine Maleate manufacturer or Chlorpheniramine Maleate supplier.
PharmaCompass also assists you with knowing the Chlorpheniramine Maleate API Price utilized in the formulation of products. Chlorpheniramine Maleate API Price is not always fixed or binding as the Chlorpheniramine Maleate Price is obtained through a variety of data sources. The Chlorpheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alunex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alunex, including repackagers and relabelers. The FDA regulates Alunex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alunex 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 Alunex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alunex supplier is an individual or a company that provides Alunex active pharmaceutical ingredient (API) or Alunex finished formulations upon request. The Alunex suppliers may include Alunex API manufacturers, exporters, distributors and traders.
click here to find a list of Alunex 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 Alunex Drug Master File in Japan (Alunex JDMF) empowers Alunex 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 Alunex JDMF during the approval evaluation for pharmaceutical products. At the time of Alunex 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 Alunex suppliers with JDMF on PharmaCompass.
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