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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Deslanoside

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 1NOBILUS ENT Tomasz Koz(')luk

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    NOBILUS ENT Tomasz Koz(')luk

    Poland
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    NOBILUS ENT Tomasz Koz(')luk

    Poland
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    Deslanoside

    Registration Number : 230MF10104

    Registrant's Address : ul. Swarzewska 45,01-821 Warszawa, POLAND

    Initial Date of Registration : 2018-08-08

    Latest Date of Registration : 2018-08-08

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    Deslanoside Manufacturers

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

    Deslanoside Suppliers

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

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

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

    Deslanoside Manufacturers | Traders | Suppliers

    Deslanoside Manufacturers, Traders, Suppliers 1
    16

    We have 1 companies offering Deslanoside

    Get in contact with the supplier of your choice:

    1. Nobilus Ent
    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.