01 2Nanjing White Whale Pharmaceutical Co. , Ltd.
02 1Piramal Pharma Limited
03 1Uquifa Mexico, S. A. de C. V.
04 1Zhejiang East Asia Pharmaceutical Co. , Ltd.
01 1Japanese Pharmacopoeia Ketoconazole
02 1Japanese Pharmacopoeia ketoconazole
03 3Ketoconazole
01 1China
02 1Spain
03 1U.S.A
04 2Blank
Japanese Pharmacopoeia Ketoconazole
Registration Number : 303MF10100
Registrant's Address : Digwal Village (Sy.Nos. 7-70, 70/1 and 70/2), Kohir Mandal, Sangareddy District-502 3...
Initial Date of Registration : 2021-07-02
Latest Date of Registration : 2021-07-02
Registration Number : 218MF10434
Registrant's Address : Calle 37 Este No. 126, CIVAC, 62578, Jiutepec, Morelos, Mexico
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2020-10-29
Registration Number : 307MF10149
Registrant's Address : Coastal industrial city, Pubagan town, Sanmen county, Zhejiang, China
Initial Date of Registration : 2025-12-04
Latest Date of Registration : 2025-12-04
Registration Number : 308MF10028
Registrant's Address : No. 29 Fangshuidong Road, Jiangbei New Area, Nanjing
Initial Date of Registration : 2026-02-06
Latest Date of Registration : 2026-02-06
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Website
Corporate PDF
Japanese Pharmacopoeia Ketoconazole
Registration Number : 304MF10078
Registrant's Address : No. 29 Fangshuidong Road, Jiangbei New Area, Nanjing
Initial Date of Registration : 2022-05-25
Latest Date of Registration : 2022-05-25
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Ketoconazole 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 Ketoconazole manufacturer or Ketoconazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ketoconazole manufacturer or Ketoconazole supplier.
PharmaCompass also assists you with knowing the Ketoconazole API Price utilized in the formulation of products. Ketoconazole API Price is not always fixed or binding as the Ketoconazole Price is obtained through a variety of data sources. The Ketoconazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A S1353_Selleck manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of S1353_Selleck, including repackagers and relabelers. The FDA regulates S1353_Selleck manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. S1353_Selleck 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 S1353_Selleck manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A S1353_Selleck supplier is an individual or a company that provides S1353_Selleck active pharmaceutical ingredient (API) or S1353_Selleck finished formulations upon request. The S1353_Selleck suppliers may include S1353_Selleck API manufacturers, exporters, distributors and traders.
click here to find a list of S1353_Selleck 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 S1353_Selleck Drug Master File in Japan (S1353_Selleck JDMF) empowers S1353_Selleck 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 S1353_Selleck JDMF during the approval evaluation for pharmaceutical products. At the time of S1353_Selleck 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 S1353_Selleck suppliers with JDMF on PharmaCompass.
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