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01 1ScinoPharm Taiwan, Ltd.
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01 1Nogitecan Hydrochloride
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01 1Taiwan
Registration Number : 307MF10045
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 741014, Taiwan
Initial Date of Registration : 2025-03-26
Latest Date of Registration : 2025-03-26
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PharmaCompass offers a list of Topotecan Hydrochloride 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 Topotecan Hydrochloride manufacturer or Topotecan Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Topotecan Hydrochloride manufacturer or Topotecan Hydrochloride supplier.
PharmaCompass also assists you with knowing the Topotecan Hydrochloride API Price utilized in the formulation of products. Topotecan Hydrochloride API Price is not always fixed or binding as the Topotecan Hydrochloride Price is obtained through a variety of data sources. The Topotecan Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hycamtin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hycamtin, including repackagers and relabelers. The FDA regulates Hycamtin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hycamtin 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 Hycamtin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hycamtin supplier is an individual or a company that provides Hycamtin active pharmaceutical ingredient (API) or Hycamtin finished formulations upon request. The Hycamtin suppliers may include Hycamtin API manufacturers, exporters, distributors and traders.
click here to find a list of Hycamtin 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 Hycamtin Drug Master File in Japan (Hycamtin JDMF) empowers Hycamtin 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 Hycamtin JDMF during the approval evaluation for pharmaceutical products. At the time of Hycamtin 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 Hycamtin suppliers with JDMF on PharmaCompass.
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