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Looking for 65-46-3 / Cytidine API manufacturers, exporters & distributors?

Cytidine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Cytidine

Synonyms

65-46-3, Cytosine riboside, 1-beta-d-ribofuranosylcytosine, 4-amino-1-beta-d-ribofuranosyl-2(1h)-pyrimidinone, 1beta-ribofuranosylcytosine, Cytidin

Cas Number

65-46-3

Unique Ingredient Identifier (UNII)

5CSZ8459RP

About Cytidine

A pyrimidine nucleoside that is composed of the base CYTOSINE linked to the five-carbon sugar D-RIBOSE.

Cytidine Manufacturers

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

Cytidine Suppliers

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

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

Cytidine USDMF

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

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

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

Cytidine GMP

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

Cytidine CoA

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

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

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