OFATUMUMAB
UNII M95KG522R0

Substance Identification & Data

This profile provides standardized clinical and technical data for Ofatumumab, uniquely identified by the FDA Unique Ingredient Identifier (UNII) M95KG522R0.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 679818-59-8 and the RxNorm Concept ID (RxCUI) 712566. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
M95KG522R0
CAS Registry Number
679818-59-8
RxNorm Concept ID

Detailed Substance Profile

Preferred Name
OFATUMUMAB
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
M95KG522R0
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
Unique identification number in the NCBI database of chemical substances.
INN ID
8606
Sequential identifier assigned via the WHO International Nonproprietary Name program.
USAN ID
WW-56
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 Ofatumumab. 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

OFATUMUMAB

Common Names & Synonyms

2F2
HUMAX-CD20
IMMUNOGLOBULIN G1, ANTI-(HUMAN CD20 (ANTIGEN))(HUMAN MONOCLONAL HUMAX-CD20 HEAVY CHAIN), DISULFIDE WITH HUMAN MONOCLONAL HUMAX-CD20 .KAPPA.-CHAIN, DIMER
IMMUNOGLOBULIN G1, ANTI-(HUMAN CD20 (ANTIGEN))(HUMAN MONOCLONAL HUMAX-CD20 HEAVY CHAIN), DISULPHIDE WITH HUMAN MONOCLONAL HUMAX-CD20 .KAPPA.-CHAIN, DIMER
OFATUMUMAB [EMA EPAR]
OFATUMUMAB [INN]
OFATUMUMAB [JAN]
OFATUMUMAB [MART.]
OFATUMUMAB [MI]
OFATUMUMAB [PURPLE BOOK CDER]
OFATUMUMAB [USAN]
OFATUMUMAB [VANDF]
OFATUMUMAB [WHO-DD]

Brand / Trade Names

ARZERRA

Technical Codes

GSK1841157
GSK-1841157
GSKI841157
HUMAX-CD20 2F2
HUMAX-CD20, 2F2
HUMAX-CD20-2F2

NDC Products Containing OFATUMUMAB

This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory: