Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
01 1M/s Aarti Pharmalabs ltd
02 1M/s Alembic Pharmaceuticals limited
03 1M/s Hetero Labs Ltd
04 1M/s Shilpa Pharma Lifesciences Ltd
05 1M/sMSN laboratories Pvt Lt
01 5Ibrutinib IH
01 1WC-0041
02 1WC-0082
03 1WC-0099
04 1WC-0147
05 1WC-0349
01 5India
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
Date of Issue : 2025-08-22
Valid Till : 2028-08-21
Written Confirmation Number : WC-0099
Address of the Firm : Plot No.E-50, 50/1 and 59/1, Unit-IV, MIDC, Tarapur-401506, Taluka: Palghar, Dis...
Date of Issue : 2025-08-22
Valid Till : 2028-08-21
Written Confirmation Number : WC-0082
Address of the Firm : Karakhadi, Plot No. 842-843, At - Karakhdi, Tal. - Padra, Dist -Vadodara, Gujara...
Date of Issue : 2025-09-03
Valid Till : 2028-08-08
Written Confirmation Number : WC-0041
Address of the Firm : Unit-I, Sy. No. 10, I.D.A, Gaddapotharam (V), Jinnaram (M), Sangareddy District,...
Date of Issue : 2025-09-19
Valid Till : 2028-05-05
Written Confirmation Number : WC-0349
Address of the Firm : Unit-II, Sy. Nos. 50, 53, 53/A, 54 & 54/A,Kardanur (Village), Patancheru (Mandal...
Date of Issue : 2026-01-01
Valid Till : 2028-07-02
Written Confirmation Number : WC-0147
Address of the Firm : 100% EOU, Plot No.33, 33A, 40 to 47,Block C, D, E, H, I& AM,Raichur Industrial G...
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A Ibrutinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ibrutinib, including repackagers and relabelers. The FDA regulates Ibrutinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ibrutinib 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 Ibrutinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ibrutinib supplier is an individual or a company that provides Ibrutinib active pharmaceutical ingredient (API) or Ibrutinib finished formulations upon request. The Ibrutinib suppliers may include Ibrutinib API manufacturers, exporters, distributors and traders.
click here to find a list of Ibrutinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Ibrutinib written confirmation (Ibrutinib WC) is an official document issued by a regulatory agency to a Ibrutinib manufacturer, verifying that the manufacturing facility of a Ibrutinib active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ibrutinib APIs or Ibrutinib finished pharmaceutical products to another nation, regulatory agencies frequently require a Ibrutinib WC (written confirmation) as part of the regulatory process.
click here to find a list of Ibrutinib suppliers with Written Confirmation (WC) on PharmaCompass.
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