TUVIRUMAB
UNII 31Z0AB5WNC

Substance Identification & Data

This profile provides standardized clinical and technical data for Tuvirumab, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 31Z0AB5WNC.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 138660-97-6 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

31Z0AB5WNC

CAS Registry Number

138660-97-6

RxNorm Concept ID

N/A

Detailed Substance Profile

Preferred Name

TUVIRUMAB

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

NCI Thesaurus

C166625

National Cancer Institute reference terminology for clinical and research data.

INN ID

6559

Sequential identifier assigned via the WHO International Nonproprietary Name program.

USAN ID

BB-54

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 Tuvirumab. 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

TUVIRUMAB

Common Names & Synonyms

IMMUNOGLOBULIN G 1 (HUMAN MONOCLONAL PE1-1 ANTI-HEPATITIS B VIRUS SURFACE ANTIGEN), DISULFIDE WITH HUMAN MONOCLONAL PE1-1 .LAMBDA.-CHAIN, DIMER

IMMUNOGLOBULIN G 1 (HUMAN MONOCLONAL PE1-1 ANTI-HEPATITIS B VIRUS SURFACE ANTIGEN), DISULFIDE WITH HUMAN MONOCLONAL PE1-1 L-CHAIN, DIMER

IMMUNOGLOBULIN G1, ANTI-(HEPATITIS B VIRUS SURFACE ANTIGEN) (HUMAN MONOCLONAL PE1-1 .GAMMA.1-CHAIN), DISULFIDE WITH HUMAN MONOCLONAL PE1-1 .LAMBDA.-CHAIN, DIMER

OSTAVIR HUMAN ANTI-HEPATITIS B

TUVIRUMAB [INN]

TUVIRUMAB [USAN]