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Looking for 58-96-8 / Uridine API manufacturers, exporters & distributors?

Uridine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Uridine

Synonyms

58-96-8, Uridin, Uracil riboside, 1-beta-d-ribofuranosyluracil, Uracil, 1-beta-d-ribofuranosyl-, Beta-uridine

Cas Number

58-96-8

Unique Ingredient Identifier (UNII)

WHI7HQ7H85

About Uridine

A ribonucleoside in which RIBOSE is linked to URACIL.

Uridine Manufacturers

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

Uridine Suppliers

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

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

Uridine USDMF

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

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

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

Uridine GMP

Uridine 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 Uridine 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 Uridine GMP manufacturer or Uridine GMP API supplier for your needs.

Uridine CoA

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

Uridine CoA mostly includes findings from lab analyses of a specific batch. For each Uridine 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.

Uridine may be tested according to a variety of international standards, such as European Pharmacopoeia (Uridine EP), Uridine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Uridine 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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