European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
01 1Polpharma
02 1Aarti Pharmalabs
03 1Dr. Reddy's Laboratories
04 1Actavis Inc
05 1Alivus Life Sciences
06 1Aurisco Pharmaceutical
07 1BDR Lifesciences
08 1Catalent Pharma Solutions
09 1Cdymax
10 1Chongqing Huapont Pharmaceutical
11 1Cipla
12 1Hansoh Pharma
13 1Hetero Drugs
14 1Laurus Labs
15 1MSN Laboratories
16 1Macleods Pharmaceuticals Limited
17 1Qingfeng Pharmaceutical Group
18 2ScinoPharm Taiwan Ltd
19 1Shandong Anhong Pharmaceutical
20 1Shilpa Medicare
21 1Sichuan Kelun Pharmaceutical
22 1Sun Pharmaceutical Industries Limited
23 1Synthon Pharmaceuticals
24 1Viatris
25 1Zhejiang Jingsheng Pharmaceutical
26 2Zydus Lifesciences
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39560
Submission : 2024-04-04
Status :
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35618
Submission : 2021-04-28
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2015-06-11
Pay. Date : 2014-12-30
DMF Number : 29117
Submission : 2015-03-31
Status :
Type : II
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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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A Xtandi (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xtandi (TN), including repackagers and relabelers. The FDA regulates Xtandi (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xtandi (TN) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Xtandi (TN) supplier is an individual or a company that provides Xtandi (TN) active pharmaceutical ingredient (API) or Xtandi (TN) finished formulations upon request. The Xtandi (TN) suppliers may include Xtandi (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Xtandi (TN) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Xtandi (TN) DMF (Drug Master File) is a document detailing the whole manufacturing process of Xtandi (TN) active pharmaceutical ingredient (API) in detail. Different forms of Xtandi (TN) DMFs exist exist since differing nations have different regulations, such as Xtandi (TN) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Xtandi (TN) DMF submitted to regulatory agencies in the US is known as a USDMF. Xtandi (TN) USDMF includes data on Xtandi (TN)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Xtandi (TN) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Xtandi (TN) suppliers with USDMF on PharmaCompass.
We have 26 companies offering Xtandi (TN)
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