Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1M/s. Aarti Pharmalabs Limited
02 1M/s Dr. Reddy's Laboratories
03 1M/s BDR Lifesciences Pvt Ltd
04 1M/s Cdymax
05 1M/s Shilpa Medicare Limited
06 1M/s. Hetro Labs Limited
07 1M/s. Laurus Labs Pvt. Ltd.,
08 1MSN Laboratories Pvt. Ltd.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Date of Issue : 2023-01-06
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm : Plot No. E-50, 50/1 and 59/1, Unit — IV, MIDC, Tarapur — 401506, Taluka: Pal...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
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PharmaCompass offers a list of Enzalutamide 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 Enzalutamide manufacturer or Enzalutamide supplier for your needs.
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PharmaCompass also assists you with knowing the Enzalutamide API Price utilized in the formulation of products. Enzalutamide API Price is not always fixed or binding as the Enzalutamide Price is obtained through a variety of data sources. The Enzalutamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A XTANDI manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of XTANDI, including repackagers and relabelers. The FDA regulates XTANDI manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. XTANDI 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 XTANDI manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A XTANDI supplier is an individual or a company that provides XTANDI active pharmaceutical ingredient (API) or XTANDI finished formulations upon request. The XTANDI suppliers may include XTANDI API manufacturers, exporters, distributors and traders.
click here to find a list of XTANDI suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A XTANDI written confirmation (XTANDI WC) is an official document issued by a regulatory agency to a XTANDI manufacturer, verifying that the manufacturing facility of a XTANDI active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting XTANDI APIs or XTANDI finished pharmaceutical products to another nation, regulatory agencies frequently require a XTANDI WC (written confirmation) as part of the regulatory process.
click here to find a list of XTANDI suppliers with Written Confirmation (WC) on PharmaCompass.
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