01 1M/s. Alembic Pharmaceuticals Limited
02 1M/s. Fresenius Kabi Oncology Ltd
03 1M/sAlembic Pharmaceuticals Limited API Division
04 1MSN Laboratories Pvt. Ltd.
01 3Ibrutinib IH
02 1Ibrutinib IHS
01 1WC-0082
02 1WC-0082A5
03 1WC-0115A3
04 1WC-0349
01 4India
Date of Issue : 2022-06-17
Valid Till : 2025-07-02
Written Confirmation Number : WC-0082
Address of the Firm : API Division Kharakhadi, Plot No. 842-843, Kharakhadi, Padra Vadodara-391 450, G...
Date of Issue : 2019-10-22
Valid Till : 2022-07-02
Written Confirmation Number : WC-0082A5
Address of the Firm : API Division Kharakhadi, Plot No. 842-843, Kharakhadi, Padra Vadodara-391 450, G...
Date of Issue : 2022-09-30
Valid Till : 2025-09-15
Written Confirmation Number : WC-0115A3
Address of the Firm : D-35, Industrial Area, Kalyani, Dist Nadia-741 235, West Bengal
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm : MIs. MSN Laboratories Private Limited, Unit-II, sv. No, 50, Kardanur (Village), ...
100
PharmaCompass offers a list of Ibrutinib 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 Ibrutinib manufacturer or Ibrutinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ibrutinib manufacturer or Ibrutinib supplier.
PharmaCompass also assists you with knowing the Ibrutinib API Price utilized in the formulation of products. Ibrutinib API Price is not always fixed or binding as the Ibrutinib Price is obtained through a variety of data sources. The Ibrutinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IMBRUVICA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IMBRUVICA, including repackagers and relabelers. The FDA regulates IMBRUVICA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IMBRUVICA 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 IMBRUVICA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A IMBRUVICA supplier is an individual or a company that provides IMBRUVICA active pharmaceutical ingredient (API) or IMBRUVICA finished formulations upon request. The IMBRUVICA suppliers may include IMBRUVICA API manufacturers, exporters, distributors and traders.
click here to find a list of IMBRUVICA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A IMBRUVICA written confirmation (IMBRUVICA WC) is an official document issued by a regulatory agency to a IMBRUVICA manufacturer, verifying that the manufacturing facility of a IMBRUVICA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting IMBRUVICA APIs or IMBRUVICA finished pharmaceutical products to another nation, regulatory agencies frequently require a IMBRUVICA WC (written confirmation) as part of the regulatory process.
click here to find a list of IMBRUVICA suppliers with Written Confirmation (WC) on PharmaCompass.
We have 3 companies offering IMBRUVICA
Get in contact with the supplier of your choice:
