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    List of Certificates of Suitability (CEPs) for MolPort-000-872-102 Active Pharmaceutical Ingredient (API) issued by the EDQM. Original Data: EDQM Database

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    MolPort-000-872-102

    APIs // Active Pharmaceutical Ingredients

    DOSSIERs // Finished Dosage Forms

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    GLOBAL SALES INFORMATION

    MARKET PLACE

    ANALYTICAL SOLUTION(s)

    PharmaCompass

    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    01 Merck KGaA Darmstadt DE (1)

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    01 Urea (1)

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    01 Germany (1)

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    01 Valid (1)

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    Merck KGaA Darmstadt DE

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    Urea

    PDF Supplier PDF
    URL Supplier Web Content
    R1-CEP 2011-045 - Rev 01
    Valid
    Chemical
    2017-11-09
    743
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    PHARMACOMPASS
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    Looking for 57-13-6 / Urea API API manufacturers, exporters & distributors?

    Urea API manufacturers, exporters & distributors 1

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

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

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

    API | Excipient name

    Urea API

    Synonyms

    Carbamide, 57-13-6, Carbonyldiamide, Isourea, Ureophil, Carbonyldiamine

    Cas Number

    57-13-6

    Unique Ingredient Identifier (UNII)

    8W8T17847W

    About Urea API

    A compound formed in the liver from ammonia produced by the deamination of amino acids. It is the principal end product of protein catabolism and constitutes about one half of the total urinary solids.

    MolPort-000-872-102 Manufacturers

    A MolPort-000-872-102 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-000-872-102, including repackagers and relabelers. The FDA regulates MolPort-000-872-102 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-000-872-102 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 MolPort-000-872-102 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

    MolPort-000-872-102 Suppliers

    A MolPort-000-872-102 supplier is an individual or a company that provides MolPort-000-872-102 active pharmaceutical ingredient (API) or MolPort-000-872-102 finished formulations upon request. The MolPort-000-872-102 suppliers may include MolPort-000-872-102 API manufacturers, exporters, distributors and traders.

    click here to find a list of MolPort-000-872-102 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

    MolPort-000-872-102 CEP

    A MolPort-000-872-102 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-000-872-102 Certificate of Suitability (COS). The purpose of a MolPort-000-872-102 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-000-872-102 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-000-872-102 to their clients by showing that a MolPort-000-872-102 CEP has been issued for it. The manufacturer submits a MolPort-000-872-102 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-000-872-102 CEP holder for the record. Additionally, the data presented in the MolPort-000-872-102 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-000-872-102 DMF.

    A MolPort-000-872-102 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-000-872-102 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

    click here to find a list of MolPort-000-872-102 suppliers with CEP (COS) on PharmaCompass.

    MolPort-000-872-102 Manufacturers | Traders | Suppliers

    MolPort-000-872-102 Manufacturers, Traders, Suppliers 1
    64

    We have 1 companies offering MolPort-000-872-102

    Get in contact with the supplier of your choice:

    1. Merck Group
    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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