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 Alka-seltzer plus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alka-seltzer plus, including repackagers and relabelers. The FDA regulates Alka-seltzer plus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alka-seltzer plus 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 Alka-seltzer plus supplier is an individual or a company that provides Alka-seltzer plus active pharmaceutical ingredient (API) or Alka-seltzer plus finished formulations upon request. The Alka-seltzer plus suppliers may include Alka-seltzer plus API manufacturers, exporters, distributors and traders.
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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 Alka-seltzer plus Drug Master File in Japan (Alka-seltzer plus JDMF) empowers Alka-seltzer plus 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 Alka-seltzer plus JDMF during the approval evaluation for pharmaceutical products. At the time of Alka-seltzer plus JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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