With Virupaksha, you get a quality product with on-time delivery.
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01 1Virupaksha Organics Limited
02 1Chunghwa Chemical Synthesis & Biotech Co. , Ltd.
03 1Daito Co., Ltd.
04 1Quimica Syntetica S. A.
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01 3Fluconazole
02 1Fluconazole (production only)
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01 1India
02 1Japan
03 1Spain
04 1Taiwan
Registration Number : 222MF10167
Registrant's Address : B-4, IDA, Gandhinagar, Hyderabad-500037, Telangana, INDIA
Initial Date of Registration : 2010-06-08
Latest Date of Registration : 2023-01-25
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Fluconazole (for manufacturing purposes only)
Registration Number : 218MF10050
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2024-06-12
Registration Number : 217MF10660
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-09-29
Latest Date of Registration : 2009-04-08
Registration Number : 306MF10038
Registrant's Address : Calle Dulcinea, s/n 28805 Alcala De Henares Madrid Spain
Initial Date of Registration : 2024-03-06
Latest Date of Registration : 2024-03-06
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PharmaCompass offers a list of Fluconazole 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 Fluconazole manufacturer or Fluconazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluconazole manufacturer or Fluconazole supplier.
PharmaCompass also assists you with knowing the Fluconazole API Price utilized in the formulation of products. Fluconazole API Price is not always fixed or binding as the Fluconazole Price is obtained through a variety of data sources. The Fluconazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TPF manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TPF, including repackagers and relabelers. The FDA regulates TPF manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TPF 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 TPF manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A TPF supplier is an individual or a company that provides TPF active pharmaceutical ingredient (API) or TPF finished formulations upon request. The TPF suppliers may include TPF API manufacturers, exporters, distributors and traders.
click here to find a list of TPF 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 TPF Drug Master File in Japan (TPF JDMF) empowers TPF 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 TPF JDMF during the approval evaluation for pharmaceutical products. At the time of TPF 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 TPF suppliers with JDMF on PharmaCompass.
We have 4 companies offering TPF
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