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Looking for 1467052-77-2 / Tazemetostat API manufacturers, exporters & distributors?

Tazemetostat manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Tazemetostat

Synonyms

1467052-75-0, Tazemetostat monohydrobromide, Epz-6438 monohydrobromide, E-7438 hydrobromide, Ez438, Tazemetostat (hydrobromide)

Cas Number

1467052-77-2

Unique Ingredient Identifier (UNII)

6P89T5M073

About Tazemetostat

Tazemetostat Hydrobromide is the hydrobromide salt form of tazemetostat, an orally available, small molecule selective and S-adenosyl methionine (SAM) competitive inhibitor of histone methyl transferase EZH2, with potential antineoplastic activity. Upon oral administration, tazemetostat selectively inhibits the activity of both wild-type and mutated forms of EZH2. Inhibition of EZH2 specifically prevents the methylation of histone H3 lysine 27 (H3K27). This decrease in histone methylation alters gene expression patterns associated with cancer pathways and results in decreased tumor cell proliferation in EZH2 mutated cancer cells. EZH2, which belongs to the class of histone methyltransferases (HMTs), is overexpressed or mutated in a variety of cancer cells and plays a key role in tumor cell proliferation.

Tazemetostat Manufacturers

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

Tazemetostat Suppliers

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

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

Tazemetostat NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Tazemetostat as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Tazemetostat API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Tazemetostat as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Tazemetostat and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tazemetostat NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Tazemetostat suppliers with NDC on PharmaCompass.

Tazemetostat GMP

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

Tazemetostat CoA

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

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

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