01 2Kongo Chemical Co., Ltd.
01 1Chlorpheniramine maleate (manufactured only)
02 1d- chlorpheniramine maleate (manufactured only)
01 2Japan
d-Chlorpheniramine maleate (for manufacturing only)
Registration Number : 217MF11197
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2008-09-09
Chlorpheniramine maleate (for manufacturing only)
Registration Number : 217MF11194
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2008-02-08
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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 Sine off manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sine off, including repackagers and relabelers. The FDA regulates Sine off manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sine off API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Sine off supplier is an individual or a company that provides Sine off active pharmaceutical ingredient (API) or Sine off finished formulations upon request. The Sine off suppliers may include Sine off API manufacturers, exporters, distributors and traders.
click here to find a list of Sine off 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 Sine off Drug Master File in Japan (Sine off JDMF) empowers Sine off 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 Sine off JDMF during the approval evaluation for pharmaceutical products. At the time of Sine off 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 Sine off suppliers with JDMF on PharmaCompass.
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