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Find Pazopanib Hydrochloride manufacturers, exporters & distributors on PharmaCompass

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  • TABLET;ORAL - EQ 200MG BASE
  • TABLET;ORAL - EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Looking for 635702-64-6 / Pazopanib Hydrochloride API manufacturers, exporters & distributors?

Pazopanib Hydrochloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Pazopanib Hydrochloride

Synonyms

635702-64-6, Pazopanib hcl, Votrient, Pazopanib (hydrochloride), Armala, Unii-33y9anm545

Cas Number

635702-64-6

Unique Ingredient Identifier (UNII)

33Y9ANM545

About Pazopanib Hydrochloride

Pazopanib Hydrochloride is the hydrochloride salt of a small molecule inhibitor of multiple protein tyrosine kinases with potential antineoplastic activity. Pazopanib selectively inhibits vascular endothelial growth factor receptors (VEGFR)-1, -2 and -3, c-kit and platelet derived growth factor receptor (PDGF-R), which may result in inhibition of angiogenesis in tumors in which these receptors are upregulated.

Pazopanib Manufacturers

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

Pazopanib Suppliers

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

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

Pazopanib USDMF

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

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

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

Pazopanib KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Pazopanib Drug Master File in Korea (Pazopanib KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pazopanib. The MFDS reviews the Pazopanib KDMF as part of the drug registration process and uses the information provided in the Pazopanib KDMF to evaluate the safety and efficacy of the drug.

After submitting a Pazopanib KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Pazopanib API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Pazopanib suppliers with KDMF on PharmaCompass.

Pazopanib WC

A Pazopanib written confirmation (Pazopanib WC) is an official document issued by a regulatory agency to a Pazopanib manufacturer, verifying that the manufacturing facility of a Pazopanib active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pazopanib APIs or Pazopanib finished pharmaceutical products to another nation, regulatory agencies frequently require a Pazopanib WC (written confirmation) as part of the regulatory process.

click here to find a list of Pazopanib suppliers with Written Confirmation (WC) on PharmaCompass.

Pazopanib 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 Pazopanib as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Pazopanib 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 Pazopanib 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 Pazopanib and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pazopanib NDC to their finished compounded human drug products, they may choose to do so.

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

Pazopanib GMP

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

Pazopanib CoA

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

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

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