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    List of Drug Master Files (JDMF) for Tox21_300611 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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    Tox21_300611

    APIs // Active Pharmaceutical Ingredients

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    01 Kongo Chemical Co., Ltd. (1)

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    01 Diphenhydramine hydrochloride (production only) (1)

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    01 Japan (1)

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    Kongo Chemical Co., Ltd.

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    Diphenhydramine hydrochloride (for manufacturing only)

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    217MF11188
    3 Himata, Toyama City, Toyama Prefe...
    2010-03-09
    2005-12-12
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    Looking for 147-24-0 / Diphenhydramine Hydrochloride API manufacturers, exporters & distributors?

    Diphenhydramine Hydrochloride manufacturers, exporters & distributors 1

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    PharmaCompass offers a list of Diphenhydramine Hydrochloride 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 Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier for your needs.

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

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

    API | Excipient name

    Diphenhydramine Hydrochloride

    Synonyms

    147-24-0, Diphenhydramine hcl, Dimedrol, Allergival, Carphenamine, Bendylate

    Cas Number

    147-24-0

    Unique Ingredient Identifier (UNII)

    TC2D6JAD40

    About Diphenhydramine Hydrochloride

    A histamine H1 antagonist used as an antiemetic, antitussive, for dermatoses and pruritus, for hypersensitivity reactions, as a hypnotic, an antiparkinson, and as an ingredient in common cold preparations. It has some undesired antimuscarinic and sedative effects.

    Tox21_300611 Manufacturers

    A Tox21_300611 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300611, including repackagers and relabelers. The FDA regulates Tox21_300611 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300611 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 Tox21_300611 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

    Tox21_300611 Suppliers

    A Tox21_300611 supplier is an individual or a company that provides Tox21_300611 active pharmaceutical ingredient (API) or Tox21_300611 finished formulations upon request. The Tox21_300611 suppliers may include Tox21_300611 API manufacturers, exporters, distributors and traders.

    click here to find a list of Tox21_300611 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

    Tox21_300611 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 Tox21_300611 Drug Master File in Japan (Tox21_300611 JDMF) empowers Tox21_300611 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 Tox21_300611 JDMF during the approval evaluation for pharmaceutical products. At the time of Tox21_300611 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 Tox21_300611 suppliers with JDMF on PharmaCompass.

    Tox21_300611 Manufacturers | Traders | Suppliers

    Tox21_300611 Manufacturers, Traders, Suppliers 1
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    We have 1 companies offering Tox21_300611

    Get in contact with the supplier of your choice:

    1. Kongo Chemical 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.
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