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