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.
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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 Chlor-trimeton 12 hour manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlor-trimeton 12 hour, including repackagers and relabelers. The FDA regulates Chlor-trimeton 12 hour manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlor-trimeton 12 hour 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 Chlor-trimeton 12 hour supplier is an individual or a company that provides Chlor-trimeton 12 hour active pharmaceutical ingredient (API) or Chlor-trimeton 12 hour finished formulations upon request. The Chlor-trimeton 12 hour suppliers may include Chlor-trimeton 12 hour API manufacturers, exporters, distributors and traders.
click here to find a list of Chlor-trimeton 12 hour 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 Chlor-trimeton 12 hour Drug Master File in Japan (Chlor-trimeton 12 hour JDMF) empowers Chlor-trimeton 12 hour 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 Chlor-trimeton 12 hour JDMF during the approval evaluation for pharmaceutical products. At the time of Chlor-trimeton 12 hour 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 Chlor-trimeton 12 hour suppliers with JDMF on PharmaCompass.
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