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    Buflomedil

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    GLOBAL SALES INFORMATION

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 1Qilu Tianhe Pharmaceutical Co., Ltd.

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    PharmaCompass

    Looking for 35543-24-9 / Buflomedil API manufacturers, exporters & distributors?

    Buflomedil manufacturers, exporters & distributors 1

    58

    PharmaCompass offers a list of Buflomedil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Buflomedil manufacturer or Buflomedil supplier for your needs.

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

    API | Excipient name

    Buflomedil

    Synonyms

    Buflomedil hcl, 35543-24-9, Fonzylane, Loftyl, Buflomedil (hydrochloride), 4-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-1-butanone hydrochloride

    Cas Number

    35543-24-9

    Unique Ingredient Identifier (UNII)

    3J944AFS8S

    Buflomedil Manufacturers

    A Buflomedil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buflomedil, including repackagers and relabelers. The FDA regulates Buflomedil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buflomedil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

    Buflomedil Suppliers

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

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

    Buflomedil USDMF

    A Buflomedil DMF (Drug Master File) is a document detailing the whole manufacturing process of Buflomedil active pharmaceutical ingredient (API) in detail. Different forms of Buflomedil DMFs exist exist since differing nations have different regulations, such as Buflomedil USDMF, ASMF (EDMF), JDMF, CDMF, etc.

    A Buflomedil DMF submitted to regulatory agencies in the US is known as a USDMF. Buflomedil USDMF includes data on Buflomedil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Buflomedil USDMF is kept confidential to protect the manufacturer’s intellectual property.

    click here to find a list of Buflomedil suppliers with USDMF on PharmaCompass.

    Buflomedil Manufacturers | Traders | Suppliers

    Buflomedil Manufacturers, Traders, Suppliers 1
    12

    We have 1 companies offering Buflomedil

    Get in contact with the supplier of your choice:

    1. Qilu Tianhe Pharmaceutical 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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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.