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Looking for 179474-81-8 / Prucalopride (USAN/INN) API manufacturers, exporters & distributors?

Prucalopride (USAN/INN) manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Prucalopride (USAN/INN) 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 Prucalopride (USAN/INN) manufacturer or Prucalopride (USAN/INN) supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prucalopride (USAN/INN) manufacturer or Prucalopride (USAN/INN) supplier.

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

API | Excipient name

Prucalopride (USAN/INN)

Synonyms

179474-81-8, Motegrity, R093877, 4-amino-5-chloro-2,3-dihydro-n-[1-(3-methoxypropyl)-4-piperidinyl]-7-benzofurancarboxamide, 4-amino-5-chloro-n-[1-(3-methoxypropyl)piperidin-4-yl]-2,3-dihydro-1-benzofuran-7-carboxamide, 4-amino-5-chloro-n-(1-(3-methoxypropyl)piperidin-4-yl)-2,3-dihydrobenzofuran-7-carboxamide

Cas Number

179474-81-8

Unique Ingredient Identifier (UNII)

0A09IUW5TP

About Prucalopride (USAN/INN)

Prucalopride is a dihydrobenzofurancarboxamide derivative from the benzofurane family that selectively stimulates 5-HT4 receptors and thus, it presents enterokinetic properties. The high selectivity of prucalopride allowed further development as it prevented the cardiac adverse reactions observed due to non-target effects of precedent therapies. Prucalopride was developed by Shire Development LLC and approved for use in Europe in 2009, in Canada on December 7, 2011 and by the FDA on December 17, 2018.

DSSTox_CID_31459 Manufacturers

A DSSTox_CID_31459 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_31459, including repackagers and relabelers. The FDA regulates DSSTox_CID_31459 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_31459 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

DSSTox_CID_31459 Suppliers

A DSSTox_CID_31459 supplier is an individual or a company that provides DSSTox_CID_31459 active pharmaceutical ingredient (API) or DSSTox_CID_31459 finished formulations upon request. The DSSTox_CID_31459 suppliers may include DSSTox_CID_31459 API manufacturers, exporters, distributors and traders.

DSSTox_CID_31459 GMP

DSSTox_CID_31459 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 DSSTox_CID_31459 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 DSSTox_CID_31459 GMP manufacturer or DSSTox_CID_31459 GMP API supplier for your needs.

DSSTox_CID_31459 CoA

A DSSTox_CID_31459 CoA (Certificate of Analysis) is a formal document that attests to DSSTox_CID_31459's compliance with DSSTox_CID_31459 specifications and serves as a tool for batch-level quality control.

DSSTox_CID_31459 CoA mostly includes findings from lab analyses of a specific batch. For each DSSTox_CID_31459 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.

DSSTox_CID_31459 may be tested according to a variety of international standards, such as European Pharmacopoeia (DSSTox_CID_31459 EP), DSSTox_CID_31459 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DSSTox_CID_31459 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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