ECROMEXIMAB
UNII M76FX2JZRM

Substance Identification & Data

This profile provides standardized clinical and technical data for Ecromeximab, uniquely identified by the FDA Unique Ingredient Identifier (UNII) M76FX2JZRM.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 292819-64-8 and the RxNorm Concept ID (RxCUI) N/A. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code

M76FX2JZRM

CAS Registry Number

292819-64-8

RxNorm Concept ID

N/A

Detailed Substance Profile

Preferred Name

ECROMEXIMAB

Official standardized name for this substance within the FDA UNII nomenclature system.

NCI Thesaurus

C61095

National Cancer Institute reference terminology for clinical and research data.

INN ID

8239

Sequential identifier assigned via the WHO International Nonproprietary Name program.

USAN ID

NN-04

Identifier assigned by the United States Adopted Names Council.

Substance Type

protein

ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Ecromeximab. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

FDA Official Name

ECROMEXIMAB

Common Names & Synonyms

ECROMEXIMAB [INN]

ECROMEXIMAB [USAN]

ECROMEXIMAB [WHO-DD]

IMMUNOGLOBULIN G1, ANTI-(GD3 GANGLIOSIDE) (HUMAN-MOUSE MONOCLONAL KM871 .GAMMA.1-CHAIN), DISULFIDE WITH HUMAN-MOUSE MONOCLONAL KM871 .KAPPA.-CHAIN, DIMER

IMMUNOGLOBULIN G1, ANTI-(GD3 GANGLIOSIDE) (HUMAN-MOUSE MONOCLONAL KM871 .GAMMA.1-CHAIN), DISULPHIDE WITH HUMAN-MOUSE MONOCLONAL KM871 .KAPPA.-CHAIN, DIMER