RETEPLASE
UNII DQA630RIE9

Substance Identification & Data

This profile provides standardized clinical and technical data for Reteplase, uniquely identified by the FDA Unique Ingredient Identifier (UNII) DQA630RIE9.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 133652-38-7 and the RxNorm Concept ID (RxCUI) 76895. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
DQA630RIE9
CAS Registry Number
133652-38-7
RxNorm Concept ID

Detailed Substance Profile

Preferred Name
RETEPLASE
Official standardized name for this substance within the FDA UNII nomenclature system.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
INN ID
7102
Sequential identifier assigned via the WHO International Nonproprietary Name program.
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 Reteplase. 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

RETEPLASE

Common Names & Synonyms

HUMAN TISSUE-TYPE PLASMINOGEN ACTIVATOR(AMINO ACIDS 1-3 AND 176-527)
HUMAN T-PA (RESIDUES 1-3 AND 176-527)
HUMAN T-PA AMINO ACIDS 1-3 AND 176-527)
RETEPLASE [EMA EPAR]
RETEPLASE [INN]
RETEPLASE [MART.]
RETEPLASE [MI]
RETEPLASE [PURPLE BOOK CDER]
RETEPLASE [USAN]
RETEPLASE [VANDF]
RETEPLASE [WHO-DD]
RETEPLASE, RECOMBINANT
RETEPLASE,RECOMBINANT [VANDF]

Brand / Trade Names

ECOKINASE
RAPILYSIN
RETAVASE
RETEVASE

Technical Codes

BM 06.022
BM-06.022
BM-06022