01 1Alives Life Sciences Limited
02 1Hetero Labs Limited
03 1MSN Laboratories Private Limited.
04 2ST Pharm Co. , Ltd.
05 1Zhejiang Huahai Pharmaceutical Co. , Ltd.
01 6Voriconazole
01 1China
02 3India
03 2South Korea
Registration Number : 225MF10092
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2013-05-08
Latest Date of Registration : 2022-03-30
Registration Number : 305MF10027
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2023-02-08
Latest Date of Registration : 2025-03-06
Registration Number : 230MF10097
Registrant's Address : Plot No: C-24, Sanath Nagar Industrial Estate, Sanath Nagar, Hyderabad, Telangana, In...
Initial Date of Registration : 2018-08-02
Latest Date of Registration : 2018-08-02
Registration Number : 302MF10132
Registrant's Address : 231, Hyeomnyeok-ro, Siheung-si, Gyeonggi-do, Korea
Initial Date of Registration : 2020-10-29
Latest Date of Registration : 2023-01-11
Registration Number : 227MF10040
Registrant's Address : 231, Hyeomnyeok-ro, Siheung-si, Gyeonggi-do, Korea
Initial Date of Registration : 2015-02-09
Latest Date of Registration : 2015-02-09
Registration Number : 306MF10092
Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China
Initial Date of Registration : 2024-07-03
Latest Date of Registration : 2024-07-03
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PharmaCompass offers a list of Voriconazole 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 Voriconazole manufacturer or Voriconazole supplier for your needs.
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PharmaCompass also assists you with knowing the Voriconazole API Price utilized in the formulation of products. Voriconazole API Price is not always fixed or binding as the Voriconazole Price is obtained through a variety of data sources. The Voriconazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SMR000466350 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SMR000466350, including repackagers and relabelers. The FDA regulates SMR000466350 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SMR000466350 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A SMR000466350 supplier is an individual or a company that provides SMR000466350 active pharmaceutical ingredient (API) or SMR000466350 finished formulations upon request. The SMR000466350 suppliers may include SMR000466350 API manufacturers, exporters, distributors and traders.
click here to find a list of SMR000466350 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 SMR000466350 Drug Master File in Japan (SMR000466350 JDMF) empowers SMR000466350 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 SMR000466350 JDMF during the approval evaluation for pharmaceutical products. At the time of SMR000466350 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 SMR000466350 suppliers with JDMF on PharmaCompass.
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