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    Clemastine (fumarate)

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

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    $ API Ref.Price (USD/KG) : 9,496Xls

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    01 1Sekisui Medical Co., Ltd.

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    Clemastine (fumarate) Manufacturers

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

    Clemastine (fumarate) Suppliers

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

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

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

    Clemastine (fumarate) Manufacturers | Traders | Suppliers

    Clemastine (fumarate) Manufacturers, Traders, Suppliers 1
    78

    We have 1 companies offering Clemastine (fumarate)

    Get in contact with the supplier of your choice:

    1. Sekisui Medical Co. Ltd
    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.