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01 1Catalent Micron Technologies, Inc.

02 2Lonza AG

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VANDETANIB

NDC Package Code : 49187-0220

Start Marketing Date : 2016-07-26

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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VANDETANIB

NDC Package Code : 49187-0221

Start Marketing Date : 2021-02-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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Looking for 443913-73-3 / VANDETANIB API manufacturers, exporters & distributors?

VANDETANIB manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

VANDETANIB

Synonyms

443913-73-3, Zactima, Zd6474, Caprelsa, N-(4-bromo-2-fluorophenyl)-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolin-4-amine, Vandetanib (zd6474)

Cas Number

443913-73-3

Unique Ingredient Identifier (UNII)

YO460OQ37K

About VANDETANIB

Vandetanib is an orally bioavailable 4-anilinoquinazoline. Vandetanib selectively inhibits the tyrosine kinase activity of vascular endothelial growth factor receptor 2 (VEGFR2), thereby blocking VEGF-stimulated endothelial cell proliferation and migration and reducing tumor vessel permeability. This agent also blocks the tyrosine kinase activity of epidermal growth factor receptor (EGFR), a receptor tyrosine kinase that mediates tumor cell proliferation and migration and angiogenesis.

VANDETANIB Manufacturers

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

VANDETANIB Suppliers

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

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

VANDETANIB 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 VANDETANIB as an active pharmaceutical ingredient (API).

Finished drug products

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

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

VANDETANIB Manufacturers | Traders | Suppliers

VANDETANIB Manufacturers, Traders, Suppliers 1
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We have 2 companies offering VANDETANIB

Get in contact with the supplier of your choice:

  1. Catalent Pharma Solutions
  2. Lonza Inc & Lonza America Inc
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.