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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 USDMF

A MolPort-000-872-102 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-000-872-102 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-000-872-102 DMFs exist exist since differing nations have different regulations, such as MolPort-000-872-102 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-000-872-102 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-000-872-102 USDMF includes data on MolPort-000-872-102's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-000-872-102 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-000-872-102 suppliers with USDMF on PharmaCompass.

MolPort-000-872-102 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 MolPort-000-872-102 Drug Master File in Japan (MolPort-000-872-102 JDMF) empowers MolPort-000-872-102 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 MolPort-000-872-102 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-000-872-102 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 MolPort-000-872-102 suppliers with JDMF 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 GMP

MolPort-000-872-102 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of MolPort-000-872-102 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right MolPort-000-872-102 GMP manufacturer or MolPort-000-872-102 GMP API supplier for your needs.

MolPort-000-872-102 CoA

A MolPort-000-872-102 CoA (Certificate of Analysis) is a formal document that attests to MolPort-000-872-102's compliance with MolPort-000-872-102 specifications and serves as a tool for batch-level quality control.

MolPort-000-872-102 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-000-872-102 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

MolPort-000-872-102 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-000-872-102 EP), MolPort-000-872-102 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-000-872-102 USP).

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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