Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs Limited
02 1Dr.Reddy's Laboratories Limited
03 1Evonik Corporation
04 1Aurisco Pharmaceutical Co.,Ltd
05 1BDR Lifesciences Private Limited
06 1Chemo Biosynthesis s.r.l.
07 1Curia New York, Inc.
08 1Hetero Labs Limited
09 1Hovione LLC
10 1Jiangsu Hansoh Pharmaceutical Group Co., Ltd.
11 1LAURUS LABS LIMITED
12 1Lonza Tampa LLC
13 1MSN Laboratories Private Limited
14 1MYLAN LABORATORIES LIMITED
15 1Optimus Drugs Private Limited
16 2ScinoPharm Taiwan Ltd.
01 2ENZALUTAMIDE
02 13Enzalutamide
03 1Enzalutamide SDD Hov A
04 1enzalutamide
01 2China
02 1Germany
03 7India
04 1Portugal
05 1Spain
06 2Taiwan
07 3U.S.A
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-1121
Start Marketing Date : 2021-04-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-976
Start Marketing Date : 2015-03-31
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
NDC Package Code : 62128-0388
Start Marketing Date : 2015-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 16812-010
Start Marketing Date : 2022-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42052-1901
Start Marketing Date : 2024-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.2kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 42385-733
Start Marketing Date : 2016-12-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0044
Start Marketing Date : 2016-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-018
Start Marketing Date : 2018-06-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1376
Start Marketing Date : 2016-11-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-876
Start Marketing Date : 2016-11-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Enzalutamide manufacturer or Enzalutamide supplier.
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.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing XTANDI as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for XTANDI API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture XTANDI as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain XTANDI and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a XTANDI NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of XTANDI suppliers with NDC on PharmaCompass.
We have 16 companies offering XTANDI
Get in contact with the supplier of your choice:
