01 1Delta Synthetic Co. , Ltd.
02 1Hamari PFST Co., Ltd.
03 1Yamamoto Chemical Industry Co., Ltd.
01 1Japanese Pharmacopoeia guaifenesin
02 2Japanese Pharmacopoeia guaifenesin (production only)
01 2Japan
02 1Taiwan
Japanese Pharmacopoeia Guaifenesin (for manufacturing only)
Registration Number : 218MF10772
Registrant's Address : 15, Minsheng St. , Tucheng Dist. , New Taipei City 23679, Taiwan (R.O.C.)
Initial Date of Registration : 2006-09-22
Latest Date of Registration : 2016-01-08
Japanese Pharmacopoeia Guaifenesin
Registration Number : 217MF10558
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-12-13
Japanese Pharmacopoeia Guaifenesin (for manufacturing only)
Registration Number : 217MF10885
Registrant's Address : Osaka Prefecture, Osaka City, Suminoe Ward, Nanko Kita 1-19-40
Initial Date of Registration : 2005-11-07
Latest Date of Registration : 2010-02-16
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PharmaCompass offers a list of Guaifenesin 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 Guaifenesin manufacturer or Guaifenesin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Guaifenesin manufacturer or Guaifenesin supplier.
PharmaCompass also assists you with knowing the Guaifenesin API Price utilized in the formulation of products. Guaifenesin API Price is not always fixed or binding as the Guaifenesin Price is obtained through a variety of data sources. The Guaifenesin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A component of Quibron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of component of Quibron, including repackagers and relabelers. The FDA regulates component of Quibron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. component of Quibron 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 component of Quibron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A component of Quibron supplier is an individual or a company that provides component of Quibron active pharmaceutical ingredient (API) or component of Quibron finished formulations upon request. The component of Quibron suppliers may include component of Quibron API manufacturers, exporters, distributors and traders.
click here to find a list of component of Quibron 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 component of Quibron Drug Master File in Japan (component of Quibron JDMF) empowers component of Quibron 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 component of Quibron JDMF during the approval evaluation for pharmaceutical products. At the time of component of Quibron 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 component of Quibron suppliers with JDMF on PharmaCompass.
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