01 1Chongqing Shenghuaxi Pharmaceutical Co. ,Ltd
02 1HETERO DRUGS LIMITED.
03 1INIST ST CO. , LTD.
04 1KOLON LIFE SCIENCE, INC.
05 1Zhejiang Charioteer Pharmaceutical Co. , Ltd.
01 5Famciclovir
01 2China
02 1India
03 2South Korea
Registration Number : 306MF10040
Registrant's Address : Tongyuanxi, Dazhan, Xianju, Zhejiang Province, 317321, P. R. China.
Initial Date of Registration : 2024-03-13
Latest Date of Registration : 2024-08-28
Registration Number : 228MF10152
Registrant's Address : No. 8 Jiangqiao Road, Nan an District Chongqing China
Initial Date of Registration : 2016-08-08
Latest Date of Registration : 2016-08-08
Registration Number : 228MF10146
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2016-08-03
Latest Date of Registration : 2016-08-03
Registration Number : 228MF10130
Registrant's Address : 500, Sinnae-ro, Geumwang-eup, Eumseong-gun, Chungcheongbuk-do, Korea
Initial Date of Registration : 2016-07-15
Latest Date of Registration : 2017-05-16
Registration Number : 228MF10115
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2016-06-21
Latest Date of Registration : 2017-05-10
11
PharmaCompass offers a list of Famciclovir 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 Famciclovir manufacturer or Famciclovir supplier for your needs.
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PharmaCompass also assists you with knowing the Famciclovir API Price utilized in the formulation of products. Famciclovir API Price is not always fixed or binding as the Famciclovir Price is obtained through a variety of data sources. The Famciclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ezovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ezovir, including repackagers and relabelers. The FDA regulates Ezovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ezovir 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 Ezovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ezovir supplier is an individual or a company that provides Ezovir active pharmaceutical ingredient (API) or Ezovir finished formulations upon request. The Ezovir suppliers may include Ezovir API manufacturers, exporters, distributors and traders.
click here to find a list of Ezovir 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 Ezovir Drug Master File in Japan (Ezovir JDMF) empowers Ezovir 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 Ezovir JDMF during the approval evaluation for pharmaceutical products. At the time of Ezovir 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 Ezovir suppliers with JDMF on PharmaCompass.
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