01 1Zhejiang Lepu Pharmaceutical Co. , Ltd.
01 1Pazopanib Hydrochloride
01 1China
Registration Number : 307MF10025
Registrant's Address : No. 29 Binhai Road, Jiaojiang District, Taizhou City, Zhejiang Province, 318000, Chin...
Initial Date of Registration : 2025-02-07
Latest Date of Registration : 2025-02-07
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PharmaCompass offers a list of Pazopanib 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 Pazopanib Hydrochloride manufacturer or Pazopanib Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pazopanib Hydrochloride manufacturer or Pazopanib Hydrochloride supplier.
PharmaCompass also assists you with knowing the Pazopanib Hydrochloride API Price utilized in the formulation of products. Pazopanib Hydrochloride API Price is not always fixed or binding as the Pazopanib Hydrochloride Price is obtained through a variety of data sources. The Pazopanib Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Votrient manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Votrient, including repackagers and relabelers. The FDA regulates Votrient manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Votrient 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 Votrient manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Votrient supplier is an individual or a company that provides Votrient active pharmaceutical ingredient (API) or Votrient finished formulations upon request. The Votrient suppliers may include Votrient API manufacturers, exporters, distributors and traders.
click here to find a list of Votrient 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 Votrient Drug Master File in Japan (Votrient JDMF) empowers Votrient 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 Votrient JDMF during the approval evaluation for pharmaceutical products. At the time of Votrient JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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