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 purposes 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
A Chlorpheniramine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorpheniramine Maleate, including repackagers and relabelers. The FDA regulates Chlorpheniramine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorpheniramine Maleate 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 Chlorpheniramine Maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorpheniramine Maleate supplier is an individual or a company that provides Chlorpheniramine Maleate active pharmaceutical ingredient (API) or Chlorpheniramine Maleate finished formulations upon request. The Chlorpheniramine Maleate suppliers may include Chlorpheniramine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorpheniramine Maleate 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 Chlorpheniramine Maleate Drug Master File in Japan (Chlorpheniramine Maleate JDMF) empowers Chlorpheniramine Maleate 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 Chlorpheniramine Maleate JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorpheniramine Maleate 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 Chlorpheniramine Maleate suppliers with JDMF on PharmaCompass.
We have 1 companies offering Chlorpheniramine Maleate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
