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    Arcol E 351

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

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    PharmaCompass

    Looking for 106392-12-5 / Detalan API manufacturers, exporters & distributors?

    Detalan manufacturers, exporters & distributors 1

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

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

    API | Excipient name

    Detalan

    Synonyms

    Poloxamer 188, 9003-11-6, Poloxamer 407, Pluronic f-68, 106392-12-5, 2-methyloxirane;oxirane

    Cas Number

    106392-12-5

    About Detalan

    A copolymer of polyethylene and polypropylene ether glycol. It is a non-ionic polyol surface-active agent used medically as a fecal softener and in cattle for prevention of bloat.

    Arcol E 351 Manufacturers

    A Arcol E 351 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arcol E 351, including repackagers and relabelers. The FDA regulates Arcol E 351 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arcol E 351 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 Arcol E 351 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.

    Arcol E 351 Suppliers

    A Arcol E 351 supplier is an individual or a company that provides Arcol E 351 active pharmaceutical ingredient (API) or Arcol E 351 finished formulations upon request. The Arcol E 351 suppliers may include Arcol E 351 API manufacturers, exporters, distributors and traders.

    click here to find a list of Arcol E 351 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.

    Arcol E 351 USDMF

    A Arcol E 351 DMF (Drug Master File) is a document detailing the whole manufacturing process of Arcol E 351 active pharmaceutical ingredient (API) in detail. Different forms of Arcol E 351 DMFs exist exist since differing nations have different regulations, such as Arcol E 351 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

    A Arcol E 351 DMF submitted to regulatory agencies in the US is known as a USDMF. Arcol E 351 USDMF includes data on Arcol E 351's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Arcol E 351 USDMF is kept confidential to protect the manufacturer’s intellectual property.

    click here to find a list of Arcol E 351 suppliers with USDMF on PharmaCompass.

    Arcol E 351 Manufacturers | Traders | Suppliers

    Arcol E 351 Manufacturers, Traders, Suppliers 1
    59

    We have 1 companies offering Arcol E 351

    Get in contact with the supplier of your choice:

    1. BASF
    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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