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    List of Drug Master Files (JDMF) for Ulipristal Acetate Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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    Ulipristal Acetate

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    Curia Spain S. A. U.

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    Ulipristal acetate micronized

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    Looking for 126784-99-4 / Ulipristal Acetate API manufacturers, exporters & distributors?

    Ulipristal Acetate manufacturers, exporters & distributors 1

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    PharmaCompass offers a list of Ulipristal Acetate 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 Ulipristal Acetate manufacturer or Ulipristal Acetate supplier for your needs.

    Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ulipristal Acetate manufacturer or Ulipristal Acetate supplier.

    PharmaCompass also assists you with knowing the Ulipristal Acetate API Price utilized in the formulation of products. Ulipristal Acetate API Price is not always fixed or binding as the Ulipristal Acetate Price is obtained through a variety of data sources. The Ulipristal Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

    API | Excipient name

    Ulipristal Acetate

    Synonyms

    126784-99-4, Cdb-2914, Ella, Ellaone, Cdb 2914, Hrp 2000

    Cas Number

    126784-99-4

    Unique Ingredient Identifier (UNII)

    YF7V70N02B

    About Ulipristal Acetate

    Ulipristal Acetate is an orally bioavailable, acetate salt of ulipristal, a selective progesterone receptor modulator with anti-progesterone activity. Ulipristal binds to the progesterone receptor (PR), thereby inhibiting PR-mediated gene expression, and interfering with progesterone activity in the reproductive system. As a result, this agent may suppress the growth of uterine leiomyomatosis. Furthermore, by inhibiting or delaying ovulation and effecting endometrial tissue, ulipristal can be used as an emergency contraception

    Ulipristal Acetate Manufacturers

    A Ulipristal Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ulipristal Acetate, including repackagers and relabelers. The FDA regulates Ulipristal Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ulipristal Acetate 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 Ulipristal Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

    Ulipristal Acetate Suppliers

    A Ulipristal Acetate supplier is an individual or a company that provides Ulipristal Acetate active pharmaceutical ingredient (API) or Ulipristal Acetate finished formulations upon request. The Ulipristal Acetate suppliers may include Ulipristal Acetate API manufacturers, exporters, distributors and traders.

    click here to find a list of Ulipristal Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

    Ulipristal Acetate 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 Ulipristal Acetate Drug Master File in Japan (Ulipristal Acetate JDMF) empowers Ulipristal Acetate 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 Ulipristal Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Ulipristal Acetate 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 Ulipristal Acetate suppliers with JDMF on PharmaCompass.

    Ulipristal Acetate Manufacturers | Traders | Suppliers

    Ulipristal Acetate Manufacturers, Traders, Suppliers 1
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    We have 1 companies offering Ulipristal Acetate

    Get in contact with the supplier of your choice:

    1. Curia
    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.
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