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    Xtandi (TN)

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    Enzalutamide

    Registration Number : 307MF10090

    Registrant's Address : No. 27, Donghai 5th Avenue, Taizhouwan Economic and Technical Development Zone, Linha...

    Initial Date of Registration : 2025-07-23

    Latest Date of Registration : 2025-07-23

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    Looking for 915087-33-1 / Enzalutamide API manufacturers, exporters & distributors?

    Enzalutamide manufacturers, exporters & distributors 1

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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.

    API | Excipient name

    Enzalutamide

    Synonyms

    915087-33-1, Mdv3100, Mdv-3100, 4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)-2-fluoro-n-methylbenzamide, Mdv 3100, Enzalutamide (mdv3100)

    Cas Number

    915087-33-1

    Unique Ingredient Identifier (UNII)

    93T0T9GKNU

    About Enzalutamide

    Enzalutamide is an orally bioavailable, organic, non-steroidal small molecule targeting the androgen receptor (AR) with potential antineoplastic activity. Through a mechanism that is reported to be different from other approved AR antagonists, enzalutamide inhibits the activity of prostate cancer cell ARs, which may result in a reduction in prostate cancer cell proliferation and, correspondingly, a reduction in the serum prostate specific antigen (PSA) level. AR over-expression in prostate cancer represents a key mechanism associated with prostate cancer hormone resistance.

    Xtandi (TN) Manufacturers

    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.

    click here to find a list of Xtandi (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

    Xtandi (TN) Suppliers

    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.

    Xtandi (TN) JDMF

    The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

    The Xtandi (TN) Drug Master File in Japan (Xtandi (TN) JDMF) empowers Xtandi (TN) API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

    PMDA reviews the Xtandi (TN) JDMF during the approval evaluation for pharmaceutical products. At the time of Xtandi (TN) JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

    click here to find a list of Xtandi (TN) suppliers with JDMF on PharmaCompass.

    Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
    For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.