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GADOBENATE DIMEGLUMINE

NDC Package Code : 57876-333

Start Marketing Date : 2004-11-23

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 127000-20-8 / Gadobenic Acid API manufacturers, exporters & distributors?

Gadobenic Acid manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Gadobenic Acid

Synonyms

Gadobenate dimeglumine, Gd-bopta/dimeg, Gadobenic acid dimeglumine salt, B-19036/7, E-7155, Q21080030

Cas Number

127000-20-8

About Gadobenic Acid

Gadobenate Dimeglumine is a gadolinium-based paramagnetic contrast agent. When placed in a magnetic field, gadobenate dimeglumine produces a large magnetic moment and so a large local magnetic field, which can enhance the relaxation rate of nearby protons; as a result, the signal intensity of tissue images observed with magnetic resonance imaging (MRI) may be enhanced. Because this agent is preferentially taken up by normal functioning hepatocytes, normal hepatic tissue is enhanced with MRI while tumor tissue is unenhanced. In addition, because gadobenate dimeglumine is excreted in the bile, it may be used to visualize the biliary system using MRI.

Multihance Multipack Manufacturers

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

Multihance Multipack Suppliers

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

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

Multihance Multipack 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 Multihance Multipack as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Multihance Multipack Manufacturers | Traders | Suppliers

Multihance Multipack Manufacturers, Traders, Suppliers 1
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We have 1 companies offering Multihance Multipack

Get in contact with the supplier of your choice:

  1. Bracco
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.