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Looking for 59-14-3 / Broxuridine API manufacturers, exporters & distributors?

Broxuridine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Broxuridine

Synonyms

59-14-3, Bromodeoxyuridine, 5-bromodeoxyuridine, 5-brdu, Brdu, Budr

Cas Number

59-14-3

Unique Ingredient Identifier (UNII)

G34N38R2N1

About Broxuridine

A nucleoside that substitutes for thymidine in DNA and thus acts as an antimetabolite. It causes breaks in chromosomes and has been proposed as an antiviral and antineoplastic agent. It has been given orphan drug status for use in the treatment of primary brain tumors.

Broxuridine Manufacturers

A Broxuridine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Broxuridine, including repackagers and relabelers. The FDA regulates Broxuridine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Broxuridine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Broxuridine Suppliers

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

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

Broxuridine USDMF

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

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

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

Broxuridine GMP

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

Broxuridine CoA

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

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

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