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Looking for 1201438-56-3 / Duvelisib API manufacturers, exporters & distributors?

Duvelisib manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Duvelisib

Synonyms

1201438-56-3, Ipi-145, Ink-1197, (s)-3-(1-((9h-purin-6-yl)amino)ethyl)-8-chloro-2-phenylisoquinolin-1(2h)-one, Ipi 145, Unii-610v23s0ji

Cas Number

1201438-56-3

Unique Ingredient Identifier (UNII)

610V23S0JI

About Duvelisib

Duvelisib is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities. Upon administration, duvelisib prevents the activation of the PI3K delta/gamma-mediated signaling pathways which may lead to a reduction in cellular proliferation in PI3K delta/gamma-expressing tumor cells. Unlike other isoforms of PI3K, the delta and gamma isoforms are overexpressed primarily in hematologic malignancies and inflammatory and autoimmune diseases. By selectively targeting these PI3K isoforms, PI3K signaling in normal, non-neoplastic cells is minimally or not affected which would result in a more favorable side effect profile.

Duvelisib Manufacturers

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

Duvelisib Suppliers

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

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

Duvelisib GMP

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

Duvelisib CoA

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

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

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