![Virtual Booth](https://www.pharmacompass.com/image/vb/vb-orange-btn.png)
![EuroAPI Header](https://www.pharmacompass.com/image/flap/euroapi-w34-desktop-headergif-72716.gif)
![EuroAPI Header](https://www.pharmacompass.com/image/flap/euroapi-w34-mob-headergif-95876.gif)
01 M/S BDR Lifesciences (1)
02 M/s Alembic Pharmaceuticals Limited (1)
03 M/s BDR Pharmaceuticals (1)
04 M/s Shilpa Medicare Limited (1)
05 M/s. Alembic Pharmaceuticals Limited (1)
06 M/s. Cipla Limited (1)
07 M/s. Hetro Labs Limited (1)
08 M/s. Natco Pharma Ltd, (1)
09 M/s. Reliance Life Sciences Pvt. Ltd. (1)
10 M/s. Shilpa Medicare Ltd., (1)
11 MSN Laboratories Pvt. Ltd. (1)
01 SORAFENIB TOSYLATE IH (2)
02 Sorafenib IH (1)
03 Sorafenib Tosylate (IH) (2)
04 Sorafenib Tosylate IH (4)
05 Sorafenib Tosylate IHS (1)
06 Sorafenib tosylate IP (1)
01 WC-0014 (1)
02 WC-0041 (1)
03 WC-0082 (1)
04 WC-0082A8 (1)
05 WC-0138 (1)
06 WC-0147 (1)
07 WC-0147A3 (1)
08 WC-0198 (1)
09 WC-0340A3 (1)
10 WC-0349 (1)
11 WC-340n (1)
01 India (11)
22
PharmaCompass offers a list of Sorafenib 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 Sorafenib manufacturer or Sorafenib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sorafenib manufacturer or Sorafenib supplier.
PharmaCompass also assists you with knowing the Sorafenib API Price utilized in the formulation of products. Sorafenib API Price is not always fixed or binding as the Sorafenib Price is obtained through a variety of data sources. The Sorafenib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nexavar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nexavar, including repackagers and relabelers. The FDA regulates Nexavar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nexavar 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 Nexavar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nexavar supplier is an individual or a company that provides Nexavar active pharmaceutical ingredient (API) or Nexavar finished formulations upon request. The Nexavar suppliers may include Nexavar API manufacturers, exporters, distributors and traders.
click here to find a list of Nexavar suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nexavar written confirmation (Nexavar WC) is an official document issued by a regulatory agency to a Nexavar manufacturer, verifying that the manufacturing facility of a Nexavar active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Nexavar APIs or Nexavar finished pharmaceutical products to another nation, regulatory agencies frequently require a Nexavar WC (written confirmation) as part of the regulatory process.
click here to find a list of Nexavar suppliers with Written Confirmation (WC) on PharmaCompass.
We have 8 companies offering Nexavar
Get in contact with the supplier of your choice: