Find Bevacizumab+Rituximab manufacturers, exporters & distributors on PharmaCompass

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Synopsis

Synopsis

ACTIVE PHARMA INGREDIENTS

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CEP/COS

CEP/COS Certifications

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JDMF

JDMFs Filed

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EU WC

EU WC

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KDMF

KDMF

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NDC API

NDC API

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VMF

NDC API

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Listed Suppliers

Other Suppliers

API REF. PRICE (USD/KG)

$
$ 0

MARKET PLACE

0INTERMEDIATES

FINISHED DOSAGE FORMULATIONS

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FDA Orange Book

FDA (Orange Book)

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Canada

Canada

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Australia

Australia

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South Africa

South Africa

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Listed Dossiers

Listed Dossiers

0 DRUGS IN DEVELOPMENT

FDF Dossiers

DRUG PRODUCT COMPOSITIONS

REF. STANDARDS OR IMPURITIES

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EDQM

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USP

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JP

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Others

PATENTS & EXCLUSIVITIES

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US Patents

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US Exclusivities

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Health Canada Patents

DIGITAL CONTENT

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Data Compilation #PharmaFlow

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Stock Recap #PipelineProspector

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Weekly News Recap #Phispers

GLOBAL SALES INFORMATION

Annual Reports

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0RELATED EXCIPIENT COMPANIES

0EXCIPIENTS BY APPLICATIONS

Chemistry

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Also known as:
Molecular Formula
C14H18ILiN2O3
Molecular Weight
396.2  g/mol
InChI Key
CNMYRBKJCDLCHB-UHFFFAOYSA-M

Bevacizumab+Rituximab
1 2D Structure

Bevacizumab+Rituximab

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
lithium;4-[2-(diethylamino)ethylcarbamoyl]-2-iodobenzoate
2.1.2 InChI
InChI=1S/C14H19IN2O3.Li/c1-3-17(4-2)8-7-16-13(18)10-5-6-11(14(19)20)12(15)9-10;/h5-6,9H,3-4,7-8H2,1-2H3,(H,16,18)(H,19,20);/q;+1/p-1
2.1.3 InChI Key
CNMYRBKJCDLCHB-UHFFFAOYSA-M
2.1.4 Canonical SMILES
[Li+].CCN(CC)CCNC(=O)C1=CC(=C(C=C1)C(=O)[O-])I
2.2 Create Date
2008-06-02
3 Chemical and Physical Properties
Molecular Weight 396.2 g/mol
Molecular Formula C14H18ILiN2O3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count7
Exact Mass396.05222 g/mol
Monoisotopic Mass396.05222 g/mol
Topological Polar Surface Area72.5 Ų
Heavy Atom Count21
Formal Charge0
Complexity340
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2

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Looking for / Bevacizumab+Rituximab API manufacturers, exporters & distributors?

Bevacizumab+Rituximab manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Bevacizumab+Rituximab 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 Bevacizumab+Rituximab manufacturer or Bevacizumab+Rituximab supplier for your needs.

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

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

API | Excipient name

Bevacizumab+Rituximab

Bevacizumab+Rituximab Manufacturers

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

Bevacizumab+Rituximab Suppliers

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

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

Bevacizumab+Rituximab USDMF

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

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

click here to find a list of Bevacizumab+Rituximab suppliers with USDMF on PharmaCompass.

Bevacizumab+Rituximab GMP

Bevacizumab+Rituximab 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 Bevacizumab+Rituximab 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 Bevacizumab+Rituximab GMP manufacturer or Bevacizumab+Rituximab GMP API supplier for your needs.

Bevacizumab+Rituximab CoA

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

Bevacizumab+Rituximab CoA mostly includes findings from lab analyses of a specific batch. For each Bevacizumab+Rituximab 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.

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